AROMATIC VINYL COMPOUND, METAL COMPLEX THEREOF, AND PREPARATION METHOD THEREFOR AND USE THEREOF

Abstract

Provided are an aromatic vinyl compound, a metal complex thereof, and a preparation method therefor and the use thereof. The aromatic vinyl compound and the metal complex thereof have an inhibitory activity on the binding of PD-1/PD-L1, and therefore the aromatic vinyl compound and the metal complex thereof can be used for treating related diseases such as tumors. In addition, the obtained metal complex can also be used as an imaging agent.

##STR00001##

Claims

1. A compound represented by general formula II or a metal complex thereof, or their tautomers thereof, or their stereoisomers thereof, or their pharmaceutically acceptable salts thereof, or their solvates thereof: ##STR00224## X.sup.1, X.sup.2, X.sup.3, X.sup.4, and X.sup.5 are each independently CH or N; R.sup.1 is hydrogen, halogen, cyano, C.sub.1-C.sub.4 alkyl, or C.sub.1-C.sub.4 alkyl substituted by one or more R.sup.a; R.sup.2 and R.sup.3 are each independently hydrogen or halogen; R.sup.4 is hydrogen, halogen, C.sub.1-C.sub.4 alkyl, or C.sub.1-C.sub.4 alkyl substituted by one or more R.sup.b; R.sup.5 and R.sup.6 are each independently hydrogen, deuterium, C.sub.1-C.sub.4 alkyl, or C.sub.1-C.sub.4 alkyl substituted by one or more R.sup.c; or, R.sup.5, R.sup.6 together with the nitrogen atom to which they are attached form a 5- to 7-membered heterocyclic ring, or a 5- to 7-membered heterocyclic ring substituted by one or more R.sup.c; in the 5- to 7-membered heterocyclic ring, the number of heteroatoms is 1, 2, 3, or 4, and each heteroatom is independently selected from N, O, and S; each R.sup.a, each R.sup.b and each R.sup.c are independently deuterium, halogen, hydroxyl, amino, C.sub.1-C.sub.4 alkyl, C.sub.1-C.sub.4 alkyl-O, COOH, or C(O)OR.sup.9; each R.sup.8 is independently hydrogen, deuterium, halogen, hydroxyl, amino, C.sub.1-C.sub.4 alkyl, C.sub.1-C.sub.4 alkyl-S, C.sub.1-C.sub.4 alkyl-O, C(O) NH.sub.2, C(O)OC.sub.1-4 alkyl, OR.sup.8a, NHR.sup.8a, NR.sup.8aR.sup.8b, NHC(O)R.sup.8d, C.sub.1-C.sub.4 alkyl substituted by one or more R.sup.8c, C.sub.1-C.sub.4 alkyl-S substituted by one or more R.sup.8c, or C.sub.1-C.sub.4 alkyl-O substituted by one or more R.sup.8c; or, two adjacent R.sup.8 together with the carbon atoms on the benzene ring to which they are attached form a 5- to 7-membered carbocyclic ring, a 5- to 7-membered heterocyclic ring, a 5- to 7-membered carbocyclic ring substituted by one or more C.sub.1-4 alkyl, or a 5- to 7-membered heterocyclic ring substituted by one or more C.sub.1-4 alkyl; in the 5- to 7-membered heterocyclic ring, the number of heteroatoms is 1, 2, 3, or 4, and each heteroatom is independently selected from N and O; each R.sup.8a, R.sup.8b, and each R.sup.8c are independently C.sub.1-C.sub.4 alkyl-S, halogen, C.sub.1-C.sub.4 alkyl, C.sub.1-C.sub.4 alkyl-O, COOH, (C.sub.1-C.sub.4 alkylene)-COOH, C(O)OC.sub.1-C.sub.4 alkyl, C(O)NH.sub.2, C(O)NHC.sub.1-C.sub.4 alkyl, 5- to 7-membered heterocyclic ring, or NR.sup.8eR.sup.8f; in the 5- to 7-membered heterocyclic ring, the species of heteroatoms are independently selected from one or more of N, O, and S, and the number of heteroatoms is independently 1, 2, or 3; R.sup.8e and R.sup.8f are each independently hydrogen, halogen, C.sub.1-C.sub.4 alkyl, or C.sub.1-C.sub.4 alkyl substituted by one or more R.sup.8g; each R.sup.8g is independently halogen, C.sub.1-C.sub.4 alkyl, hydroxyl, NR.sup.8hR.sup.8k, C.sub.1-C.sub.4 alkyl-O, COOH, (C.sub.1-C.sub.4 alkylene)-COOH, C(O)OC.sub.1-C.sub.4 alkyl, C(O)NH.sub.2, or C(O)NHC.sub.1-C.sub.4 alkyl; R.sup.8h and R.sup.8k are each independently hydrogen or C.sub.1-C.sub.4 alkyl; each R.sup.8d is independently C.sub.6-C.sub.10 aryl substituted by one or more R.sup.8d-1, or 5- to 10-membered heteroaryl substituted by one or more R.sup.8d-2; in the 5- to 10-membered heteroaryl, the species of heteroatoms are independently selected from one or more of N, O, and S, and the number of heteroatoms is independently 1, 2, or 3; each R.sup.8d-1 and R.sup.8d-2 are independently C.sub.1-C.sub.4 alkoxy or C.sub.1-C.sub.4 alkyl substituted by one or more R.sup.8d-1-1; each R.sup.8d-1-1 is independently 5- to 7-membered heterocyclic ring substituted by one carboxyl; in the 5- to 7-membered heterocyclic ring, the species of heteroatoms are independently selected from one or more of N, O, and S, and the number of heteroatoms is independently 1, 2, or 3; q is 0, 1, 2, or 3; L.sup.1 is (i) a single bond or (CH.sub.2).sub.n; (ii) (CH.sub.2).sub.m, in which 1, 2, 3, 4, or 5 non-adjacent CH.sub.2 are independently replaced by Y.sub.1, and each Y.sub.1 is independently C(O), C(O)O, O, NH, C(O)NH, or NHC(O)NH; or (iii) (CH.sub.2).sub.p, in which one CH.sub.2 is replaced by Y.sub.2, and the other 0, 1, 2, 3, or 4 non-adjacent CH.sub.2 are independently replaced by Y.sub.3; each Y.sub.3 is independently C(O), C(O)O, O, NH, C(O)NH, or NHC(O)NH; Y.sub.2 is 5- to 7-membered carbocyclic ring or 5- to 7-membered heterocyclic ring; in the 5- to 7-membered heterocyclic ring, the number of heteroatoms is 1, 2, 3, or 4, and each heteroatom is independently selected from N, O, and S; L.sup.1 is unsubstituted or 1, 2, or 3 H contained in L.sup.1 are each independently substituted by R.sup.7; n, m, and p are each independently 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, or 14; each R.sup.7 is independently C.sub.1-C.sub.4 alkyl or -L.sup.3-R.sup.9; L.sup.3 is (i) (CH.sub.2).sub.j; or (ii) (CH.sub.2).sub.k, in which 1, 2, 3, or 4 non-adjacent CH.sub.2 are independently replaced by Y.sub.4, and each Y.sub.4 is independently C(O), C(O)O, O, NH, C(O)NH, or NHC(O)NH; L.sup.3 is unsubstituted or 1, 2, or 3 H contained in L.sup.3 are each independently substituted by R.sup.10; j and k are each independently 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, or 14; R.sup.9 is hydrogen, C.sub.6-C.sub.10 aryl, or C.sub.6-C.sub.10 aryl substituted by one or more R.sup.d; each R.sup.10 is independently C.sub.1-C.sub.4 alkyl; each R.sup.d is independently C.sub.1-C.sub.4 alkyl or C.sub.1-C.sub.4 alkyl substituted by one or more R.sup.e; each R.sup.e is independently hydroxyl, amino, C.sub.1-C.sub.4 alkyl, C.sub.1-C.sub.4 alkyl-O, COOH, or C(O)OR.sup.h; R.sup.g and R.sup.h are each independently C.sub.1-C.sub.4 alkyl or halogenated C.sub.1-C.sub.4 alkyl; L.sup.2 is metal chelating group; the metal complex is a complex chelated by the compound represented by general formula II with a metal atom or ion.

2. The compound represented by general formula II or the metal complex thereof, or their tautomers thereof, or their stereoisomers thereof, or their pharmaceutically acceptable salts thereof, or their solvates thereof according to claim 1, wherein, it satisfies one or more of the following conditions: a) q is 0, 1, or 2; each R.sup.8 is independently C.sub.1-C.sub.4 alkyl, NHC(O)R.sup.8d, or C.sub.1-C.sub.4 alkyl-O substituted by one or more R.sup.8c; each R.sup.c is independently 5- to 7-membered heterocyclic ring; in the 5- to 7-membered heterocyclic ring, the species of heteroatoms are independently selected from one or more of N, O, and S, and the number of heteroatoms is independently 1, 2, or 3; each R.sup.8d is independently C.sub.6-C.sub.10 aryl substituted by one or more R.sup.8d-1, or 5- to 10-membered heteroaryl substituted by one or more R.sup.8d-2; in the 5- to 10-membered heteroaryl, the species of heteroatoms are independently selected from one or more of N, O, and S, and the number of heteroatoms is independently 1, 2, or 3; each R.sup.8d-1 and R.sup.8d-2 are independently C.sub.1-C.sub.4 alkoxy or C.sub.1-C.sub.4 alkyl substituted by one or more R.sup.8-d-1; each R.sup.8d-1-1 is independently 5- to 7-membered heterocyclic ring substituted by one carboxyl; in the 5- to 7-membered heterocyclic ring, the species of heteroatoms are independently selected from one or more of N, O, and S, and the number of heteroatoms is independently 1, 2, or 3; b) R.sup.1 is cyano or C.sub.1-C.sub.4 alkyl; X.sup.1, X.sup.2, and X.sup.3 are each independently CH or N; c) R.sup.2 and R.sup.3 are hydrogen; d) R.sup.4 is C.sub.1-C.sub.4 alkyl or C.sub.1-C.sub.4 alkyl substituted by one or more R.sup.b; each R.sup.b is independently halogen; X.sup.4 and X.sup.5 are each independently CH or N; e) R.sup.5, R.sup.6 together with the nitrogen atom to which they are attached form a 5- to 7-membered heterocyclic ring substituted by one or more R.sup.c; in the 5- to 7-membered heterocyclic ring, the number of heteroatoms is 1, 2, 3, or 4, and each heteroatom is independently selected from N, O, and S; R.sup.c is COOH; f) L.sup.1 is (ii) (CH.sub.2).sub.m, in which 1, 2, 3, 4, or 5 non-adjacent CH.sub.2 are independently replaced by Y.sub.1, and each Y.sub.1 is independently C(O)O, O, or C(O)NH; or (iii) (CH.sub.2).sub.p, in which one CH.sub.2 is replaced by Y.sub.2, and the other 1, 2, 3, or 4 non-adjacent CH.sub.2 are independently replaced by Y.sub.3; each Y.sub.3 is independently C(O), O, or C(O)NH; Y.sub.2 is 5- to 7-membered carbocyclic ring or 5- to 7-membered heterocyclic ring; in the 5- to 7-membered heterocyclic ring, the number of heteroatoms is 1, 2, 3, or 4, and each heteroatom is independently selected from N, O, and S; L.sup.1 is unsubstituted or one H contained in L.sup.1 is each independently substituted by R.sup.7; m and p are each independently 5, 6, 7, 8, 9, 10, or 11; R.sup.7 is -L.sup.3-R.sup.9; L.sup.3 is (ii) (CH.sub.2).sub.k, in which 1, 2, 3, or 4 non-adjacent CH.sub.2 are independently replaced by Y.sub.4, and each Y.sub.4 is C(O)NH; L.sup.3 is unsubstituted; k is 7, 8, or 9; R.sup.9 is C.sub.6-C.sub.10 aryl substituted by one or more R.sup.d; each R.sup.d is independently C.sub.1-C.sub.4 alkyl; g) the metal complex is a complex chelated by the compound represented by general formula II with the metal ion; h) the metal ion does not bind to non-metal nuclide.

3. The compound represented by general formula II or the metal complex thereof, or their tautomers thereof, or their stereoisomers thereof, or their pharmaceutically acceptable salts thereof, or their solvates thereof above according to claim 2, wherein, it satisfies one or more of the following conditions: i) q is 0; j) R.sup.1 is cyano or C.sub.1-C.sub.4 alkyl; X.sup.1 and X.sup.2 are CH, and X.sup.3 is N; k) R.sup.4 is C.sub.1-C.sub.4 alkyl or C.sub.1-C.sub.4 alkyl substituted by one or more R.sup.b; each R.sup.b is independently halogen; X.sup.4 and X.sup.5 are each independently CH.

4. The compound represented by general formula II or the metal complex thereof, or their tautomers thereof, or their stereoisomers thereof, or their pharmaceutically acceptable salts thereof, or their solvates thereof according to claim 1, wherein, the definition of which is any one of the following schemes: scheme 1: X.sup.1, X.sup.2, X.sup.3, X.sup.4, and X.sup.5 are each independently CH or N; R.sup.1 is cyano or C.sub.1-C.sub.4 alkyl; R.sup.2 and R.sup.3 are hydrogen; R.sup.4 is C.sub.1-C.sub.4 alkyl or C.sub.1-C.sub.4 alkyl substituted by one or more R.sup.b; each R.sup.b is independently halogen; R.sup.5, R.sup.6 together with the nitrogen atom to which they are attached form a 5- to 7-membered heterocyclic ring substituted by one or more R.sup.c; in the 5- to 7-membered heterocyclic ring, the number of heteroatoms is 1, 2, 3, or 4, and each heteroatom is independently selected from N, O, and S; R.sup.c is COOH; q is 0, 1, or 2; each R.sup.8 is independently C.sub.1-C.sub.4 alkyl, NHC(O)R.sup.8d, or C.sub.1-C.sub.4 alkyl-O substituted by one or more R.sup.8c; each R.sup.8c is independently 5- to 7-membered heterocyclic ring; in the 5- to 7-membered heterocyclic ring, the species of heteroatoms are independently selected from one or more of N, O, and S, and the number of heteroatoms is independently 1, 2, or 3; each R.sup.8d is independently C.sub.6-C.sub.10 aryl substituted by one or more R.sup.8d-1, or 5- to 10-membered heteroaryl substituted by one or more R.sup.8d-2; in the 5- to 10-membered heteroaryl, the species of heteroatoms are independently selected from one or more of N, O, and S, and the number of heteroatoms is independently 1, 2, or 3; each R.sup.8d-1 and R.sup.8d-2 are independently C.sub.1-C.sub.4 alkoxy or C.sub.1-C.sub.4 alkyl substituted by one or more R.sup.8d-1-1; each R.sup.8d-1-1 is independently 5- to 7-membered heterocyclic ring substituted by one carboxyl; in the 5- to 7-membered heterocyclic ring, the species of heteroatoms are independently selected from one or more of N, O, and S, and the number of heteroatoms is independently 1, 2, or 3; L.sup.1 is (ii) (CH.sub.2).sub.m, in which 1, 2, 3, 4, or 5 non-adjacent CH.sub.2 are independently replaced by Y.sub.1, and each Y.sub.1 is independently C(O)O, O, or C(O)NH; or (iii) (CH.sub.2).sub.p, in which one CH.sub.2 is replaced by Y.sub.2, and the other 1, 2, 3, or 4 non-adjacent CH.sub.2 are independently replaced by Y.sub.3; each Y.sub.3 is independently C(O), O, or C(O)NH; Y.sub.2 is 5- to 7-membered carbocyclic ring or 5- to 7-membered heterocyclic ring; in the 5- to 7-membered heterocyclic ring, the number of heteroatoms is 1, 2, 3, or 4, and each heteroatom is independently selected from N, O, and S; L.sup.1 is unsubstituted or one H contained in L.sup.1 is each independently substituted by R.sup.7; m and p are each independently 5, 6, 7, 8, 9, 10, or 11; R.sup.7 is -L.sup.3-R.sup.9; L.sup.3 is (ii) (CH.sub.2).sub.k, in which 1, 2, 3, or 4 non-adjacent CH.sub.2 are independently replaced by Y.sub.4, and each Y.sub.4 is C(O)NH; L.sup.3 is unsubstituted; k is 7, 8, or 9; R.sup.9 is C.sub.6-C.sub.10 aryl substituted by one or more R.sup.d; each R.sup.d is independently C.sub.1-C.sub.4 alkyl; L.sup.2 is metal chelating group; the metal complex is a complex chelated by the compound represented by general formula II with the metal atom or ion; scheme 2: X.sup.1, X.sup.2, X.sup.4 and X.sup.5 are CH; X.sup.3 is CH or N; R.sup.1 is cyano or C.sub.1-C.sub.4 alkyl; R.sup.2 and R.sup.3 are hydrogen; R.sup.4 is C.sub.1-C.sub.4 alkyl or C.sub.1-C.sub.4 alkyl substituted by one or more R.sup.b; each R.sup.b is independently halogen; R.sup.5, R.sup.6 together with the nitrogen atom to which they are attached form a 5- to 7-membered heterocyclic ring substituted by one or more R.sup.c; in the 5- to 7-membered heterocyclic ring, the number of heteroatoms is 1, 2, 3, or 4, and each heteroatom is independently selected from N, O, and S; R.sup.c is COOH; q is 0; L.sup.1 is (ii) (CH.sub.2).sub.m, in which 1, 2, 3, 4, or 5 non-adjacent CH.sub.2 are independently replaced by Y.sub.1, and each Y.sub.1 is independently C(O)O, O, or C(O)NH; or (iii) (CH.sub.2).sub.p, in which one CH.sub.2 is replaced by Y.sub.2, and the other 1, 2, 3, or 4 non-adjacent CH.sub.2 are independently replaced by Y.sub.3; each Y.sub.3 is independently C(O), O, or C(O)NH; Y.sub.2 is 5- to 7-membered carbocyclic ring or 5- to 7-membered heterocyclic ring; in the 5- to 7-membered heterocyclic ring, the number of heteroatoms is 1, 2, 3, or 4, and each heteroatom is independently selected from N, O, and S; L.sup.1 is unsubstituted or one H contained in L.sup.1 is each independently substituted by R.sup.7; m and p are each independently 5, 6, 7, 8, 9, 10, or 11; R.sup.7 is -L.sup.3-R.sup.9; L.sup.3 is (ii) (CH.sub.2).sub.k, in which 1, 2, 3, or 4 non-adjacent CH.sub.2 are independently replaced by Y.sub.4, and each Y.sub.4 is C(O)NH; L.sup.3 is unsubstituted; k is 7, 8, or 9; R.sup.9 is C.sub.6-C.sub.10 aryl substituted by one or more R.sup.d; each R.sup.d is independently C.sub.1-C.sub.4 alkyl; L.sup.2 is metal chelating group; the metal complex is a complex chelated by the compound represented by general formula II with the metal ion.

5. The compound represented by general formula II or the metal complex thereof, or their tautomers thereof, or their stereoisomers thereof, or their pharmaceutically acceptable salts thereof, or their solvates thereof according to claim 1, wherein, it satisfies one or more of the following conditions: 1) the stereoisomer is chiral isomer; m) the metal complex has a structure represented by the following general formula I: ##STR00225## wherein, M is the metal atom or ion; n) in R.sup.1, the C.sub.1-C.sub.4 alkyl is methyl or ethyl; o) in R.sup.4, the C.sub.1-C.sub.4 alkyl is methyl or ethyl; p) in R.sup.4, the C.sub.1-C.sub.4 alkyl in the C.sub.1-C.sub.4 alkyl substituted by one or more R.sup.b is methyl or ethyl; q) in R.sup.b, the halogen is fluorine or chlorine; r) in the 5- to 7-membered heterocyclic ring substituted by one or more R.sup.c, which is formed by R.sup.5, R.sup.6 together with the nitrogen atom they are attached, the 5- to 7-membered heterocyclic ring is a 6-membered saturated monocyclic heterocyclic ring; s) in the 5- to 7-membered heterocyclic ring substituted by one or more R.sup.c, which is formed by R.sup.5, R.sup.6 together with the nitrogen atom they are attached, the number of heteroatoms is 1; t) in the 5- to 7-membered heterocyclic ring substituted by one or more R.sup.c, which is formed by R.sup.5, R.sup.6 together with the nitrogen atom they are attached, the heteroatom is N; u) L.sup.1 is connected to ring A through Y.sub.1, and Y.sub.1 connected to ring A is O; v) L.sup.1 is connected to L.sup.2 via CH.sub.2; w) L.sup.1 is O(CH.sub.2).sub.n2, O(CH.sub.2).sub.n2O(CH.sub.2).sub.m2, O(CH.sub.2).sub.n2O(CH.sub.2).sub.m2O(CH.sub.2).sub.m3, O(CH.sub.2).sub.n2OC(O)(CH.sub.2).sub.m2, O(CH.sub.2).sub.n2NHC(O)(CH.sub.2).sub.m2, O(CH.sub.2).sub.n2NHC(O)(CH.sub.2).sub.n3NHC(O)(CH.sub.2).sub.m3, O(CH.sub.2).sub.n2O(CH.sub.2).sub.n3NHC(O)(CH.sub.2).sub.n4NHC(O)(CH.sub.2).sub.m3, O(CH.sub.2).sub.n2NHC(O)Y.sub.2(CH.sub.2).sub.n3NHC(O)(CH.sub.2).sub.m3, O(CH.sub.2).sub.n2Y.sub.2C(O)(CH.sub.2).sub.m3, O(CH.sub.2).sub.n2NHC(O)Y.sub.2C(O)(CH.sub.2).sub.m3, or O(CH.sub.2).sub.n2NHC(O)Y.sub.2(CH.sub.2).sub.n3NHC(O)(CH.sub.2).sub.n4NHC(O)(CH.sub.2).sub.m3; the right end of L.sup.1 is connected to L.sup.2; each n2, each n3, each n4, each m2 and each m3 are independently 1, 2, 3, 4, 5, or 6; L.sup.1 is unsubstituted or one H contained in L.sup.1 is substituted by R.sup.7; x) when Y.sub.2 is 5- to 7-membered carbocyclic ring, the 5- to 7-membered carbocyclic ring is ##STR00226## y) when Y.sub.2 is 5- to 7-membered heterocyclic ring, the 5- to 7-membered heterocyclic ring is ##STR00227## z) R.sup.9 is phenyl or phenyl substituted by one or more R.sup.d; aa) in R.sup.d, the C.sub.1-C.sub.4 alkyl is methyl or ethyl; bb) L.sup.2 is R.sup.11 or -L.sup.4-(CH.sub.2).sub.sR.sup.11; s is 1, 2, or 3; L.sup.4 is 5- to 7-membered carbocyclic ring or 5- to 7-membered heterocyclic ring; in the 5- to 7-membered heterocyclic ring, the number of heteroatoms is 1, 2, 3, or 4, and each heteroatom is independently selected from N, O, and S; R.sup.11 is 8- to 20-membered saturated monocyclic or bridged carbocyclic ring, and 3, 4, 5, or 6 non-adjacent CH.sub.2 of the monocyclic or bridged carbocyclic ring are independently replaced by Y.sub.5, and each Y.sub.5 is independently O, NH, or N(R.sup.11a); each R.sup.11a is independently C.sub.1-C.sub.4 alkyl or C.sub.1-C.sub.4 alkyl substituted by one or more COOH; when L.sup.2 is -L.sup.4-(CH.sub.2).sub.sR.sup.11, the -L.sup.4-(CH.sub.2).sub.sR.sup.11 is ##STR00228## each Y.sub.5 is independently NH or N(R.sup.11a); each R.sup.11a is independently C.sub.1-C.sub.4 alkyl substituted by one or more COOH; cc) in the metal complex, the molar ratio of the compound represented by general formula II to the metal atom or ion is 1:1; dd) the metal ion is ion of the following metals: Al, Cu, Ga, Y, Zr, Tc, In, Lu, Re, At, Bi, or Tl; ee) the valence state of the metal ion is monovalent, divalent, trivalent, or tetravalent; ff) the metal ion is radioactive metal ion or non-radioactive metal ion; gg) the metal ion further binds to non-metal nuclide; hh) the metal ion is radioactive as a whole.

6. The compound represented by general formula II or the metal complex thereof, or their tautomers thereof, or their stereoisomers thereof, or their pharmaceutically acceptable salts thereof, or their solvates thereof according to claim 5, wherein, it satisfies one or more of the following conditions: ii) the metal complex has the structure represented by the following general formula I: ##STR00229## wherein, M is the metal ion; jj) in R.sup.4, the C.sub.1-C.sub.4 alkyl substituted by one or more R.sup.b is trifluoromethyl; kk) in the 5- to 7-membered heterocyclic ring substituted by one or more R.sup.c, which is formed by R.sup.5, R.sup.6 together with the nitrogen atom they are attached, the 5- to 7-membered heterocyclic ring is piperidine ring; ll) m2 is 1 or 2; mm) m3 is 1 or 2; nn) when Y.sub.2 is 5- to 7-membered carbocyclic ring, the 5- to 7-membered carbocyclic ring is ##STR00230## oo) when Y.sub.2 is 5- to 7-membered heterocyclic ring, the 5- to 7-membered heterocyclic ring is ##STR00231## pp) R.sup.7 is ##STR00232## qq) L.sup.2 is R.sup.11; rr) in L.sup.4, the 5- to 7-membered carbocyclic ring is ##STR00233## ss) in R.sup.11, the 8- to 20-membered is 8-, 9-, 10-, 11-, 12-, 13-, 14-, 15-, or 16-membered; tt) in R.sup.11, the C.sub.1-C.sub.4 alkyl substituted by one or more COOH is CH.sub.2COOH; uu) the metal ion is ion of the following metals: .sup.27Al, .sup.63Cu, .sup.64Cu, .sup.68Ga, .sup.70Ga, .sup.89Y, .sup.90Y, .sup.89Zr, .sup.91Zr, .sup.99mTc, .sup.111In, .sup.113n, .sup.175Lu, .sup.177Lu, .sup.186Re, .sup.188Re, .sup.211At, .sup.212Bi, .sup.213Bi, .sup.201Tl, or .sup.203Tl; vv) the valence state of the metal ion is trivalent; ww) the non-metal nuclide is radioactive non-metal nuclide or non-radioactive non-metal nuclide, and the radioactive non-metal nuclide for example .sup.18F.

7. The compound represented by general formula II or the metal complex thereof, or their tautomers thereof, or their stereoisomers thereof, or their pharmaceutically acceptable salts thereof, or their solvates thereof according to claim 6, wherein, it satisfies one or more of the following conditions: xx) the 5- to 7-membered heterocyclic ring substituted by one or more R.sup.c, which is formed by R.sup.5, R.sup.6, and together with the nitrogen atom they are attached is ##STR00234## yy) when Y.sub.2 is 5- to 7-membered carbocyclic ring, the 5- to 7-membered carbocyclic ring is ##STR00235## zz) L.sup.2 is ##STR00236## wherein the c-terminal is connected to L.sup.1; aaa) the metal ion is [Al.sup.18F].sup.2+, [.sup.68GaCl].sup.2+, [.sup.177LuCl].sup.2+, .sup.68Ga.sup.3+, or .sup.177Lu.sup.3+.

8. The compound represented by general formula II or the metal complex thereof, or their tautomers thereof, or their stereoisomers thereof, or their pharmaceutically acceptable salts thereof, or their solvates thereof according to claim 1, wherein, it satisfies one or more of the following conditions: bbb) ##STR00237## ##STR00238## is ccc) L.sup.1 is ##STR00239## ##STR00240## wherein the upper end is connected to ring A and the lower end is connected to L.sup.2; ddd) L.sup.2 is ##STR00241## eee) the L.sup.2 and the metal ion form any one of the following groups: ##STR00242##

9. The compound represented by general formula II or the metal complex thereof, or their tautomers thereof, or their stereoisomers thereof, or their pharmaceutically acceptable salts thereof, or their solvates thereof according to claim 1, wherein: ##STR00243## X.sup.1, X.sup.2, X.sup.3, X.sup.4, and X.sup.5 are each independently CH or N; R.sup.1 is hydrogen, halogen, cyano, C.sub.1-C.sub.4 alkyl, or C.sub.1-C.sub.4 alkyl substituted by one or more R.sup.a; R.sup.2 and R.sup.3 are each independently hydrogen or halogen; R.sup.4 is hydrogen, halogen, C.sub.1-C.sub.4 alkyl or C.sub.1-C.sub.4 alkyl substituted by one or more R.sup.b; R.sup.5 and R.sup.6 are each independently hydrogen, deuterium, C.sub.1-C.sub.4 alkyl, or C.sub.1-C.sub.4 alkyl substituted by one or more R.sup.c; or, R.sup.5, R.sup.6 together with the nitrogen atom to which they are attached form a 5- to 7-membered heterocyclic ring, or a 5- to 7-membered heterocyclic ring substituted by one or more R.sup.c; in the 5- to 7-membered heterocyclic ring, the number of heteroatoms is 1, 2, 3, or 4, and each heteroatom is independently selected from N, O, and S; each R.sup.a, each R.sup.b and each R.sup.c are independently deuterium, halogen, hydroxyl, amino, C.sub.1-C.sub.4 alkyl, C.sub.1-C.sub.4 alkyl-O, COOH, or C(O)OR.sup.9; each R.sup.8 is independently hydrogen, deuterium, halogen, hydroxyl, amino, C.sub.1-C.sub.4 alkyl, C.sub.1-C.sub.4 alkyl-S, C.sub.1-C.sub.4 alkyl-O, C(O)ONH.sub.2, C(O)OC.sub.1-4 alkyl, OR.sup.8a, NHR.sup.8a, NR.sup.8a, NR.sup.8aR.sup.8b C.sub.1-C.sub.4 alkyl substituted by one or more R.sup.8c, C.sub.1-C.sub.4 alkyl-S substituted by one or more R.sup.8c, or C.sub.1-C.sub.4 alkyl-O-substituted by one or more R.sup.8c; or, two adjacent R.sup.8 together with the carbon atoms on the benzene ring to which they are attached form a 5- to 7-membered carbocyclic ring, a 5- to 7-membered heterocyclic ring, a 5- to 7-membered carbocyclic ring substituted by one or more C.sub.1-4 alkyl, or a 5- to 7-membered heterocyclic ring substituted by one or more C.sub.1-4 alkyl; in the 5- to 7-membered heterocyclic ring, the number of heteroatoms is 1, 2, 3, or 4, and each heteroatom is independently selected from N and O; each R.sup.8a, R.sup.8b, and each R.sup.8c are independently C.sub.1-C.sub.4 alkyl-S, halogen, C.sub.1-C.sub.4 alkyl, C.sub.1-C.sub.4 alkyl-O, COOH, (C.sub.1-C.sub.4 alkylene)-COOH, C(O)OC.sub.1-C.sub.4 alkyl, C(O)NH.sub.2, C(O)NHC.sub.1-C.sub.4 alkyl, or NR.sup.8eR.sup.8f; R.sup.8e and R.sup.8f are each independently hydrogen, halogen, C.sub.1-C.sub.4 alkyl, or C.sub.1-C.sub.4 alkyl substituted by one or more R.sup.8g; each R.sup.8g is independently halogen, C.sub.1-C.sub.4 alkyl, hydroxyl, NR.sup.8hR.sup.8k, C.sub.1-C.sub.4 alkyl-O, COOH, (C.sub.1-C.sub.4 alkylene)-COOH, C(O)OC.sub.1-C.sub.4 alkyl, C(O)NH.sub.2, or C(O)NHC.sub.1-C.sub.4 alkyl; R.sup.8h and R.sup.8k are each independently hydrogen or C.sub.1-C.sub.4 alkyl; q is 0, 1, 2, or 3; L.sup.1 is (i) a single bond or (CH.sub.2).sub.n; (ii) (CH.sub.2).sub.m, in which 1, 2, 3, 4, or 5 non-adjacent CH.sub.2 are independently replaced by Y.sub.1, and each Y.sub.1 is independently C(O), C(O)O, O, NH, C(O)NH, or NHC(O)NH; or (iii) (CH.sub.2).sub.p, in which one CH.sub.2 is replaced by Y.sub.2, and the other 0, 1, 2, 3, or 4 non-adjacent CH.sub.2 are independently replaced by Y.sub.3; each Y.sub.3 is independently C(O), C(O)O, O, NH, C(O)NH, or NHC(O)NH; Y.sub.2 is 5- to 7-membered carbocyclic ring or 5- to 7-membered heterocyclic ring; in the 5- to 7-membered heterocyclic ring, the number of heteroatoms is 1, 2, 3, or 4, and each heteroatom is independently selected from N, O, and S; L.sup.1 is unsubstituted or 1, 2, or 3 H contained in L.sup.1 are each independently substituted by R.sup.7; n, m, and p are each independently 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, or 14; each R.sup.7 is independently C.sub.1-C.sub.4 alkyl or -L.sup.3-R.sup.9; L.sup.3 is (i) (CH.sub.2).sub.j; or (ii) (CH.sub.2).sub.k, in which 1, 2, 3, or 4 non-adjacent CH.sub.2 are independently replaced by Y.sub.4, and each Y.sub.4 is independently C(O), C(O)O, O, NH, C(O)NH, or NHC(O)NH; L.sup.3 is unsubstituted or 1, 2, or 3 H contained in L.sup.3 are each independently substituted by R.sup.10; j and k are each independently 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, or 14; R.sup.9 is hydrogen, C.sub.6-C.sub.10 aryl, or C.sub.6-C.sub.10 aryl substituted by one or more R.sup.d; each R.sup.10 is independently C.sub.1-C.sub.4 alkyl; each R.sup.d is independently C.sub.1-C.sub.4 alkyl or C.sub.1-C.sub.4 alkyl substituted by one or more R.sup.e; each R.sup.e is independently hydroxyl, amino, C.sub.1-C.sub.4 alkyl, C.sub.1-C.sub.4 alkyl-O, COOH, or C(O)OR.sup.h; R.sup.g and R.sup.h are each independently C.sub.1-C.sub.4 alkyl or halogenated C.sub.1-C.sub.4 alkyl; L.sup.2 is metal chelating group; the metal complex is a complex chelated by the compound represented by general formula II with the metal atom or ion.

10. The compound represented by general formula II or the metal complex thereof, or their tautomers thereof, or their stereoisomers thereof, or their pharmaceutically acceptable salts thereof, or their solvates thereof according to claim 1, wherein, the compound represented by general formula II or the metal complex thereof satisfies any one of the following schemes: scheme 1: the metal is Cu, Ga, Y, Zr, Tc, In, Lu, Re, At, Bi, Tl, or their radioactive or non-radioactive isotopes thereof; and/or, the valence state of the metal ion is monovalent, divalent, trivalent, or tetravalent; and/or, X.sup.1 is CH; and/or, X.sup.2 is CH; and/or, X.sup.3 is CH; and/or, X.sup.4 is CH; and/or, X.sup.5 is CH; and/or, q is 0; and/or, R.sup.1 is cyano or C.sub.1-C.sub.4 alkyl; and/or, R.sup.2 is hydrogen; and/or, R.sup.3 is hydrogen; and/or, R.sup.4 is C.sub.1-C.sub.4 alkyl or C.sub.1-C.sub.4 alkyl substituted by one or more R.sup.b; and/or, each R.sup.b is independently halogen; and/or, when R.sup.5, R.sup.6 together with the nitrogen atom to which they are attached form a 5- to 7-membered heterocyclic ring or a 5- to 7-membered heterocyclic ring substituted by one or more R.sup.c, the 5- to 7-membered heterocyclic ring is piperidine; and/or, n, m, and p are each independently 5, 6, 7, 8, 9, 10, 11, or 12; and/or, L.sup.1 is a single bond, (CH.sub.2).sub.n1NH(CH.sub.2).sub.m1, (CH.sub.2).sub.n1O(CH.sub.2).sub.m1, (CH.sub.2).sub.n1NHC(O)NH(CH.sub.2).sub.m1, O(CH.sub.2).sub.n1NH, O(CH.sub.2).sub.n1O, O(CH.sub.2).sub.n1O(CH.sub.2).sub.m1O, NH(CH.sub.2).sub.n1NH(CH.sub.2).sub.m1NH, NH(CH.sub.2).sub.n1O(CH.sub.2).sub.m1O, NH(CH.sub.2).sub.n1NH(CH.sub.2).sub.m1O, O(CH.sub.2).sub.n1NH(CH.sub.2).sub.m1O, O(CH.sub.2).sub.n1O(CH.sub.2).sub.m1NH, O(CH.sub.2).sub.n1NH(CH.sub.2).sub.m1NH, NH(CH.sub.2).sub.n1O(CH.sub.2).sub.m1NH, OY.sub.2(CH.sub.2).sub.n1NH, O(CH.sub.2).sub.n2OC(O)(CH.sub.2).sub.m2, O(CH.sub.2).sub.n2O(CH.sub.2).sub.m2, O(CH.sub.2).sub.n2NHC(O)(CH.sub.2).sub.m2, O(CH.sub.2).sub.n2NHC(O)(CH.sub.2).sub.n3NHC(O)(CH.sub.2).sub.m3, O(CH.sub.2).sub.n2Y.sub.2C(O)(CH.sub.2).sub.m2, O(CH.sub.2).sub.n2NHC(O)Y.sub.2(CH.sub.2).sub.n3NHC(O)(CH.sub.2).sub.m3, O(CH.sub.2).sub.n2NHC(O)Y.sub.2C(O)(CH.sub.2).sub.m3, O(CH.sub.2).sub.n2Y.sub.2C(O)(CH.sub.2).sub.m3, O(CH.sub.2).sub.n2NHC(O)Y.sub.2(CH.sub.2).sub.n3NHC(O)(CH.sub.2).sub.n4NHC(O)(CH.sub.2).sub.m3, O(CH.sub.2).sub.n2NHC(O)(CH.sub.2).sub.n3NHC(O)(CH.sub.2).sub.m3, or O(CH.sub.2).sub.n2O(CH.sub.2).sub.n3NHC(O)(CH.sub.2).sub.n4NHC(O)(CH.sub.2).sub.m3, each n1, each n2, each n3, n4, each m1, each m2 and each m3 are each independently 1, 2, 3, 4, 5, or 6; L.sup.1 is unsubstituted or 1, 2, or 3 H contained in L.sup.1 are each independently substituted by R.sup.7; and/or when Y.sub.2 is 5- to 7-membered carbocyclic ring, the 5- to 7-membered carbocyclic ring is; ##STR00244## and/or, when Y.sub.2 is 5- to 7-membered heterocyclic ring, the 5- to 7-membered heterocyclic ring is ##STR00245## and/or, L.sup.2 is R.sup.11 or -L.sup.4-(CH.sub.2).sub.sR.sup.11; s is 1, 2, or 3; L.sup.4 is 5- to 7-membered carbocyclic ring or 5- to 7-membered heterocyclic ring; in the 5- to 7-membered heterocyclic ring, the number of heteroatoms is 1, 2, 3, or 4, and each heteroatom is independently selected from N, O, and S; R.sup.11 is 8- to 20-membered saturated monocyclic or bridged carbocyclic ring, and 3, 4, 5, or 6 non-adjacent CH.sub.2 of the monocyclic or bridged carbocyclic ring are independently replaced by Y.sub.5; each Y.sub.5 is independently O, NH, or N(R.sup.11a); each R.sup.11a is independently C.sub.1-C.sub.4 alkyl or C.sub.1-C.sub.4 alkyl substituted by one or more COOH; and/or, each R.sup.7 is independently -L.sup.3-R.sup.9; and/or, each Y.sub.4 is independently C(O)NH; and/or, L.sup.3 is (CH.sub.2).sub.k, in which one CH.sub.2 is replaced by Y.sub.4; L.sup.3 is unsubstituted or 1, 2, or 3 H contained in L.sup.3 are each independently substituted by R.sup.10; and/or, j and k are each independently 7, 8, or 9; and/or, R.sup.9 is phenyl or phenyl substituted by one or more R.sup.d; and/or, each R.sup.d is independently C.sub.1-C.sub.4 alkyl; scheme 2: the metal is .sup.63Cu, .sup.64Cu, .sup.68Ga, .sup.70Ga, .sup.89Y, .sup.90Y, .sup.89Zr, .sup.91Zr, .sup.99mTc, .sup.111In, .sup.113In, .sup.175Lu, .sup.177Lu, .sup.186Re, .sup.188Re, .sup.211At, .sup.212Bi, .sup.213Bi, .sup.201Tl, or .sup.203Tl; and/or, X.sup.1, X.sup.2, X.sup.3, X.sup.4, and X.sup.5 are CH; and/or, R.sup.1 is cyano or methyl; and/or, R.sup.4 is methyl or trifluoromethyl, and/or, R.sup.5, R.sup.6 together with the nitrogen atom to which they are attached form ##STR00246## and/or, each R.sup.c is independently COOH; and/or, L.sup.1 is connected to ring A through Y.sub.1, and Y.sub.1 connected to ring A is O; and/or, L.sup.1 is connected to L.sup.2 via CH.sub.2; and/or, L.sup.1 is unsubstituted or one H contained in L.sup.1 is substituted by R.sup.7; and/or, R.sup.7 is ##STR00247## and/or, when Y.sub.2 is 5- to 7-membered carbocyclic ring, the 5- to 7-membered carbocyclic ring is ##STR00248## and/or, when Y.sub.2 is 5- to 7-membered heterocyclic ring, the 5- to 7-membered heterocyclic ring is ##STR00249## and/or, L.sup.2 is ##STR00250## and each R.sup.11b is independently H or R.sup.11a; each R.sup.11a is independently C.sub.1-C.sub.4 alkyl or C.sub.1-C.sub.4 alkyl substituted by one or more COOH; scheme 3: the metal complex is a complex chelated by the compound represented by general formula II with the metal ion; and/or, the metal is Ga, Lu, or their radioactive or non-radioactive isotopes thereof; and/or, R.sup.5, R.sup.6 together with the nitrogen atom to which they are attached form ##STR00251## and/or, when Y.sub.2 is 5- to 7-membered carbocyclic ring, the 5- to 7-membered carbocyclic ring is ##STR00252## and/or, L.sup.1 is ##STR00253## ##STR00254## ##STR00255## ##STR00256## wherein the a-terminal is connected to ring A and the b-terminal is connected to L.sup.2; and/or, L.sup.2 is ##STR00257## wherein the c-terminal is connected to L.sup.1; scheme 4: the metal ion is Ga.sup.3+ and Lu.sup.3+; and/or, L.sup.1 is ##STR00258## ##STR00259## ##STR00260## wherein the a-terminal is connected to ring A and the b-terminal is connected to L.sup.2; preferably, L.sup.1 is ##STR00261## ##STR00262## wherein the a-terminal is connected to ring A and the b-terminal is connected to L.sup.2; and/or, L.sup.2 is ##STR00263## where the c-terminal is connected to L.sup.1; scheme 5: the metal complex has the following structure: ##STR00264## M is a trivalent metal ion.

11-14. (canceled)

15. The compound represented by general formula II or the metal complex thereof, or their tautomers thereof, or their stereoisomers thereof, or their pharmaceutically acceptable salts thereof, or their solvates thereof according to claim 1, wherein, the C.sub.1-C.sub.4 alkyl is independently methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, or tert-butyl at any one occurrence; and/or, the one or more is independently 1, 2, 3, 4, 5, or 6 at any one occurrence; and/or, the C.sub.6-C.sub.10 aryl is independently phenyl or naphthyl at any one occurrence; and/or, the 5- to 7-membered carbocyclic ring is independently 5, 6, or 7-membered saturated monocyclic carbocyclic ring at any one occurrence; and/or, the 5- to 7-membered heterocyclic ring is independently 5, 6, or 7-membered saturated monocyclic heterocyclic ring at any one occurrence; and/or, the halogen is independently F, Cl, Br, or I at any one occurrence.

16. The compound represented by general formula II or the metal complex thereof, or their tautomers thereof, or their stereoisomers thereof, or their pharmaceutically acceptable salts thereof, or their solvates thereof according to claim 1, wherein, the compound represented by the general formula II has any one of the following structures: ##STR00265## ##STR00266## ##STR00267## ##STR00268## ##STR00269## ##STR00270## ##STR00271## ##STR00272## ##STR00273## ##STR00274## ##STR00275## ##STR00276## or, the metal complex is a complex formed by any one of the following compounds with .sup.177Lu.sup.3+: ##STR00277## ##STR00278## ##STR00279## ##STR00280## ##STR00281## ##STR00282## ##STR00283## ##STR00284## ##STR00285## or, the metal complex is a complex formed by any one of the following compounds with .sup.68Ga.sup.3+: ##STR00286## ##STR00287## ##STR00288## ##STR00289## ##STR00290## ##STR00291## ##STR00292## ##STR00293## ##STR00294## or, the metal complex is a complex formed by any one of the following compounds with [Al.sup.18F].sup.2+: ##STR00295## ##STR00296## ##STR00297## or the metal complex is a complex formed by any one of the following compounds with [.sup.68GaCl].sup.2+: ##STR00298## ##STR00299## ##STR00300## or, the metal complex is a complex formed by any one of the following compounds with [.sup.177LuCl].sup.2+: ##STR00301## ##STR00302##

17. The compound represented by general formula II or the metal complex thereof, or their tautomers thereof, or their stereoisomers thereof, or their pharmaceutically acceptable salts thereof, or their solvates thereof according to claim 1, wherein, the metal complex has any one of the following structures: ##STR00303## ##STR00304## ##STR00305## ##STR00306## ##STR00307## ##STR00308## ##STR00309## ##STR00310## ##STR00311## ##STR00312## ##STR00313## ##STR00314## ##STR00315## ##STR00316## ##STR00317## ##STR00318## ##STR00319## ##STR00320##

18. A method for preparing a metal complex of the compound represented by general formula II, wherein, the metal complex of the compound represented by general formula II has a structure represented by general formula I, which comprises the following steps: in a solvent, reacting the compound represented by the general formula II with M metal halide in the presence or absence of a buffer, to obtain the metal complex represented by the general formula I; ##STR00321## M is the metal atom or ion, and the other variables are defined as in claim 1.

19. A method for preparing the compound represented by the general formula II according to claim 1, which comprises the following steps: in a solvent, removing the Boc protective group of the compound represented by the general formula III in the presence of acid, to obtain the compound represented by the general formula II; ##STR00322## in formula II, L.sup.2 is R.sup.11 or -L.sup.4-(CH.sub.2).sub.sR.sup.11; in formula III, L.sup.20 is R.sup.110 or -L.sup.4-(CH.sub.2).sub.sR.sup.110; s is 1, 2, or 3; L.sup.4 is 5- to 7-membered carbocyclic ring or 5- to 7-membered heterocyclic ring; in the 5- to 7-membered heterocyclic ring, the number of heteroatoms is 1, 2, 3, or 4, and each heteroatom is independently selected from N, O, and S; R.sup.11 is 8- to 20-membered (for example 8-, 9-, 10-, 11-, 12-, 13-, 14-, 15-, or 16-membered) saturated monocyclic or bridged carbocyclic ring; the 3, 4, 5, or 6 non-adjacent CH.sub.2 of the monocyclic or bridged carbocyclic ring are independently replaced by Y.sub.5, and each Y.sub.5 is independently O, NH, or N(R.sup.11a); R.sup.110 is 8- to 20-membered (for example 8-, 9-, 10-, 11-, 12-, 13-, 14-, 15-, or 16-membered) saturated monocyclic or bridged carbocyclic ring, and the 3, 4, 5, or 6 non-adjacent CH.sub.2 of the monocyclic or bridged carbocyclic ring are independently replaced by Y.sub.6, and each Y.sub.6 is independently O, NH, or N(R.sup.12a); each R.sup.11a is independently C.sub.1-C.sub.4 alkyl or C.sub.1-C.sub.4 alkyl substituted by one or more COOH (for example, (C.sub.1-C.sub.4 alkylene)-COOH, for example, CH.sub.2COOH); each R.sup.12a is independently C.sub.1-C.sub.4 alkyl or C.sub.1-C.sub.4 alkyl substituted by one or more COO.sup.tBu (for example, (C.sub.1-C.sub.4 alkylene)-COOBu, for example, CH.sub.2COOBu); in formula II and formula III, R.sup.5, R.sup.6 together with the nitrogen atom to which they are attached form ##STR00323##

20. A compound represented by general formula III: ##STR00324## each variable is as defined in claim 19.

21. A compound represented by any one of the following: ##STR00325## ##STR00326## ##STR00327## ##STR00328## ##STR00329## ##STR00330## ##STR00331## ##STR00332## ##STR00333## ##STR00334## ##STR00335## ##STR00336## ##STR00337## ##STR00338## ##STR00339## ##STR00340## ##STR00341## ##STR00342## ##STR00343##

22. A pharmaceutical composition comprising the compound represented by the general formula II or the metal complex thereof, or their tautomers thereof, or their stereoisomers thereof, or their pharmaceutically acceptable salts thereof, or their solvates thereof according to claim 1, and at least one pharmaceutical excipient.

23. A method for treating or radiodiagnosing tumor in a subject in need thereof, comprising administering the compound represented by the general formula II or the metal complex thereof, or their tautomers thereof, or their stereoisomers thereof, or their pharmaceutically acceptable salts thereof, or their solvates thereof according to claim 1; preferably, the metal complex is a complex chelated by the compound represented by general formula II and a radioactive metal ion; the radioactive metal ion is radioactive metal ion for treatment or radioactive metal ion for diagnosis.

24. The method according to claim 23, wherein, the tumor is lung cancer, gastric cancer, colorectal cancer, cervical cancer, ovarian cancer, prostate cancer, breast cancer, pancreatic cancer, liver cancer, bladder cancer, renal cancer, bone cancer, skin cancer, melanoma, glioma, glioblastoma, leukemia, or lymphoma.

Description

DESCRIPTION OF DRAWINGS

[0341] FIG. 1 is a graph of the effect of compound 78 on tumor inhibition.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

[0342] The present disclosure is further illustrated below by means of examples, but the present disclosure is not limited to the scope of the examples. The experimental methods for which specific conditions are not indicated in the following examples are selected according to conventional methods and conditions, or according to the product instructions.

Main Experimental Instruments:

[0343] Radioactivity meter (CRC-55tR type); electronic balance (YP30002); germanium-gallium generator (20 mCi); vortex mixer (MX-F); HPLC (1200); TLC (Scan-RAM); gamma radioimmunoassay counter (GC-2016); UV spectrophotometer (T6 New Century);

Embodiment 1

(S,E)-2,2,2-(10-(2-(2-(2-((2-carboxypiperidin-1-yl)methyl)-5-(2-(2-cyano-[1,1-biphenyl]-3-yl)vinyl)-4-methylphenoxy)ethoxy)-2-oxoethyl)-1,4,7,10-tetraazacyclododecan-1,4,7-triyl)triacetic acid (Compound 1)

##STR00123##

Synthesis of Compound 1-e

[0344] 3-Bromo-4-methylphenol (3.74 g, 20 mmol), paraformaldehyde (4.41 g, 152 mmol), magnesium chloride (2.86 g, 30 mmol), and triethylamine (7.56 g, 75 mmol) were dissolved in acetonitrile (150 mL), and the reaction solution was heated and stirred at 80 C. for 4 hours. The reaction solution was cooled to room temperature, diluted with water (500 mL), and the pH was adjusted to 2-3 with 1 M hydrochloric acid. The mixture was extracted with ethyl acetate (500 mL2). The organic phases were combined, washed with saturated brine (200 mL1), and the organic phases were concentrated under reduced pressure. The obtained residue was separated and purified by silica gel column chromatography (petroleum ether: ethyl acetate=50:1) to obtain white solid 1-e (2.45 g, yield: 57%).

Synthesis of Compound 1-d

[0345] 1-e (645 mg, 3.0 mmol), (2-bromoethoxy) (tert-butyl) dimethylsilane (1.08 g, 4.5 mmol), and potassium carbonate (829 mg, 6.0 mmol) were dissolved in N, N-dimethylformamide (5 mL), and the reaction solution was heated at 60 C. for 16 hours. The reaction solution was cooled to room temperature and diluted with water (50 mL). The obtained mixture was extracted with ethyl acetate (50 mL2). The organic phase was washed sequentially with water (50 mL2) and saturated brine (20 mL2), dried over anhydrous sodium sulfate, and the organic phase was concentrated under reduced pressure. The obtained residue was separated and purified by silica gel column chromatography (petroleum ether: ethyl acetate=20:1) to obtain white solid 1-d (767 mg, yield: 68%).

Synthesis of Compound 1-c

[0346] Compound 1-d (373 mg, 1.0 mmol), (E)-3-(2-(4,4,5,5-tetramethyl-1,3,2-dioxyboran-2-yl)vinyl)-[1,1-biphenyl]-2-carbonitrile (397 mg, 1.2 mmol), [1,1-bis(diphenylphosphino)ferrocene]dichloropalladium (73 mg, 0.1 mmol) and potassium carbonate (276 mg, 2.0 mmol) were dissolved in 1,4-dioxane (5 mL) and water (0.5 mL), and the reaction solution was heated and stirred at 90 C. for 16 hours. The reaction solution was cooled to room temperature, and the reaction solution was diluted with saturated brine (20 mL). The resulting mixture was extracted with dichloromethane (30 mL3). The organic phases were combined, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The obtained residue was separated and purified by silica gel column chromatography (petroleum ether:ethyl acetate=5:1) to obtain yellow solid 1-c (355 mg, yield: 71%).

[0347] LC-MS (ESI): m/z=498.5(M+H).sup.+.

Synthesis of Compound 1-b

[0348] Compound 1-c (75 mg, 0.15 mmol) and (S)-piperidine-2-carboxylic acid (39 mg, 0.30 mmol) were dissolved in methanol (1 mL) and tetrahydrofuran (1 mL), and sodium cyanoborohydride (38 mg, 0.60 mmol) was added. The reaction solution was stirred at 60 C. for 1 hour. The reaction solution was cooled to room temperature and concentrated under reduced pressure, and tetrahydrofuran (1 mL), water (0.2 mL), and trifluoroacetic acid (0.5 mL) were added to the reaction solution, and the reaction solution was stirred at room temperature for 1 hour. The reaction solution was concentrated under reduced pressure, and the residue was purified by pre-HPLC to obtain white solid 1-b (48.3 mg, yield: 53%).

[0349] LC-MS (ESI): m/z=497.5 (M+H).sup.+;

[0350] .sup.1H-NMR (400 MHz, DMSO) : 8.05 (d, J=8.0 Hz, 1H), 7.79 (t, J=7.9 Hz, 1H), 7.67 (d, J=16.0 Hz, 1H), 7.63-7.47 (m, 6H), 7.40 (d, J=16.0 Hz, 1H), 7.27 (s, 2H), 7.07 (s, 1H), 4.13-3.90 (m, 5H), 3.75 (t, J=4.6 Hz, 2H), 3.28-3.21 (m, 1H), 3.08-3.00 (m, 1H), 2.38 (s, 3H), 1.97-1.86 (m, 1H), 1.78-1.66 (m, 1H), 1.63-1.48 (m, 3H), 1.45-1.31 (m, 1H).

Synthesis of Compound 1-a

[0351] Compound 1-b (40 mg, 0.08 mmol) and triethylamine (65 mg, 0.64 mmol) were dissolved in dichloromethane (1 mL). The reaction solution was cooled to 0 C., and 2-bromoacetyl bromide (19 mg, dissolved in 1 mL of dichloromethane) and tert-butyl 2,2,2-(1,4,7,10-tetraazacyclododecan-1,4,7-triyl) triacetate (206 mg, 0.40 mmol) were added to the reaction solution sequentially. The reaction solution was raised to room temperature and stirred at room temperature for 5 hours. The reaction solution was concentrated under reduced pressure and the obtained residue was separated by reversed-phase preparative chromatography (column xBridge C18, 19*150 mm*5 um; mobile phase: water (0.1% trifluoroacetic acid), methanol; gradient: 65%-80% (initial mobile phase was 35% water/65% methanol, and ending mobile phase was 20% water/80% methanol, wherein % refers to volume percentage); 13 min; flow rate 15 mL/min) to obtain white solid 1-a (22 mg, yield: 26%).

[0352] LC-MS (ESI): m/z=1051.87(M+H).sup.+.

Synthesis of Compound 1

[0353] Compound 1-a (22 mg, 0.021 mmol) was dissolved in dichloromethane (1 mL), and trifluoroacetic acid (2 mL) was added, and the reaction solution was stirred at room temperature for 16 hours. The reaction solution was concentrated under reduced pressure and the obtained residue was separated by reversed-phase preparative chromatography (column xBridge C18, 19*150 mm*5 um; mobile phase: water (0.1% trifluoroacetic acid), methanol; gradient: 65%-80% (initial mobile phase was 35% water/65% methanol, and ending mobile phase was 20% water/80% methanol, wherein % refers to volume percentage); 13 min; flow rate 15 mL/min) to obtain white solid 1 (7 mg, yield: 38%). LC-MS (ESI): m/z=883.8(M+H).sup.+;

[0354] .sup.1H-NMR (400 MHz, DMSO) : 8.05 (d, J=8.2 Hz, 1H), 7.79 (t, J=7.9 Hz, 1H), 7.66 (d, J=16.1 Hz, 1H), 7.62-7.47 (m, 6H), 7.39 (d, J=16.0 Hz, 1H), 7.28 (d, J=6.1 Hz, 2H), 4.56-4.41 (m, 1H), 4.39-4.21 (m, 3H), 4.08-3.96 (m, 1H), 3.82-3.40 (m, 15H), 3.11-2.73 (m, 16H), 2.38 (s, 3H), 2.36-2.28 (m, 1H), 1.94-1.62 (m, 3H), 1.59-1.33 (m, 3H).

Embodiment 2

(2S)-1-({4-[(1E)-2-(2-Methyl-3-phenylphenyl)vinyl]-5-(trifluoromethyl)-2-{[2-({2-({2-[4,7,10-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecan-1-yl]ethyl}oxy)ethyl]oxy}phenyl}methyl)hexahydropyridine-2-carboxylic acid (Compound 2)

##STR00124##

Synthesis of Compound 2-e

[0355] (2S)-Hexahydropyridine-2-carboxylic acid (20 g, 154.847 mmol) was dissolved in 2-methylpropan-2-yl acetate (313.727 mL, 2322.701 mmol), and perchloric acid (18.630 mL, 309.693 mmol) was added. The reaction solution was stirred at room temperature overnight. The reaction solution was concentrated under reduced pressure, and the obtained residue was diluted with ethyl acetate (50 mL), and the pH was adjusted to 9-10 with saturated sodium carbonate solution, and the mixture was washed sequentially with water (50 mL2) and saturated brine (50 mL1). The organic phase was dried and concentrated under reduced pressure to obtain 2-e (23.24 g, yield: 81.00%).

Synthesis of Compound 2-d

[0356] 3-Bromo-4-(trifluoromethyl) phenol (10.96 g, 45.475 mmol) was dissolved in toluene (200 mL), 2-e (12.64 g, 68.213 mmol) and paraformaldehyde (2.73 g, 90.951 mmol) were added to the reaction solution, and the reaction was heated and stirred at 110 C. for 6 hours. The reaction solution was cooled to room temperature, and the reaction solution was diluted with ethyl acetate (50 mL), and washed sequentially with water (50 mL2) and saturated brine (50 mL1). The organic phase was dried, and concentrated under reduced pressure to obtain 2-d (15.26 g, yield: 76.57%).

Synthesis of Compound 2-c

[0357] 4,4,5,5-Tetramethyl-2-[(1E)-2-(2-methyl-3-phenylphenyl)vinyl]-1,3,2-dioxyborane (9.00 g, 28.092 mmol) was dissolved in dioxane (160 mL) and water (4 mL), and compound 2-d (10.26 g, 23.410 mmol), [1,1-bis(diphenylphosphino)ferrocene]dichloropalladium (2.02 g, 2.341 mmol), and sodium carbonate (6.20 g, 58.524 mmol) were added to the reaction solution, and the reaction solution was heated and stirred at 80 C. for 12 hours. The reaction solution was cooled to room temperature, and the reaction solution was diluted with ethyl acetate (50 mL), and washed sequentially with water (50 mL2) and saturated brine (50 mL1). The organic phase was dried and concentrated to obtain 2-c (10.78 g, yield: 83.50%).

Synthesis of Compound 2-b

[0358] Compound 2-c (551.65 mg, 1.0 mmol) and 1-bromo-2-[(2-bromoethyl)oxy]ethane (695.73 mg, 3.000 mmol) were dissolved in N, N-dimethylformamide (5 mL), and potassium carbonate (276.42 mg, 2.000 mmol) was added, and the reaction solution was stirred for at 70 C. for 3 hours. The reaction solution was cooled to room temperature, and the reaction solution was diluted with ethyl acetate (50 mL), washed sequentially with water (20 mL2) and saturated brine (20 mL2). The organic phase was separated, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was separated by column chromatography (petroleum ether:ethyl acetate=5:1) to obtain product 2-b (548 mg, yield: 77.99%).

Synthesis of Compound 2-a

[0359] Compound 2-b (400 mg, 0.569 mmol) and tert-butyl 2,2,2-(1,4,7,10-tetraazacyclododecan-1,4,7-triyl) triacetate (292.87 mg, 0.569 mmol) were dissolved in acetonitrile (4 mL), and potassium carbonate (78.68 mg, 0.569 mmol) was added. The reaction solution was stirred at 60 C. for 16 hours. The reaction solution was cooled to room temperature, concentrated under reduced pressure, and separated by silica gel column chromatography (acetic acid in methanol:dichloromethane=1:10) to obtain 2-a (450 mg, yield: 69.56%).

Synthesis of Compound 2

[0360] Compound 2-a was dissolved in dichloromethane (4 mL), and trifluoroacetic acid (4 mL, 0.510 mmol) was added. The reaction solution was stirred at room temperature for 16 hours. The reaction solution was concentrated under reduced pressure, and the residue was purified by Prep-HPLC to obtain 2 (153 mg, yield: 42.37%).

[0361] .sup.1H-NMR (400 MHz, MeOD) : 7.89 (s, 1H), 7.66 (d, J=15.8 Hz, 1H), 7.59 (s, 1H), 7.54 (d, J=7.5 Hz, 1H), 7.46-7.39 (m, 2H), 7.38-7.24 (m, 5H), 7.18 (d, J=6.9 Hz, 1H), 4.61 (d, J=13.0 Hz, 1H), 4.50-4.37 (m, 3H), 4.00-3.83 (m, 4H), 3.77-3.56 (m, 7H), 3.53-3.26 (m, 9H), 3.25-2.98 (m, 11H), 2.35-2.29 (m, 3H), 2.25 (d, J=15.2 Hz, 1H), 2.02-1.51 (m, 5H).

Embodiment 3

(2S)-1-({4-[(1E)-2-(2-Methyl-3-phenylphenyl)vinyl]-5-(trifluoromethyl)-2-{[2-({2-[4,7,10-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecan-1-yl]acetyl}amino)ethyl]oxy}phenyl}methyl)hexahydropyridine-2-carboxylic acid (Compound 3)

##STR00125##

Synthesis of Compound 3-c

[0362] Compound 2-c (22.53 mg, 0.05 mmol), 2-(2-bromoethyl) isoindole-1,3-dione (508.16 mg, 2.000 mmol) and potassium carbonate (276.40 mg, 2.000 mmol) were dissolved in N, N-dimethylformamide (5 mL). The reaction solution was heated and stirred at 60 C. for 16 hours, and the reaction solution was cooled to room temperature, and the reaction solution was directly separated by C18 reversed-phase column chromatography to obtain a mixture of product and raw material 3-c (450 mg), which was directly put into the next step of reaction.

Synthesis of Compound 3-b

[0363] Compound 3-c (450 mg, 0.174 mmol) and hydrazine hydrate (10.89 mg, 0.174 mmol) were dissolved in methanol (5 mL). The reaction solution was heated and stirred at 65 C. for 2 hours. The reaction solution was cooled to room temperature, and the reaction solution was directly separated by prep-HPLC to obtain product 3-b (35 mg, yield: 33.82%).

Synthesis of Compound 3-a

[0364] Compound 3-b (35 mg, 0.059 mmol), (10-{1-[(methylpropan-2-yl)oxy]-1-oxoethyl-2-yl}-4,7-bis{2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl}-1,4,7,10-tetraazacyclododecan-1-yl)acetic acid (40.45 mg, 0.071 mmol) and HBTU reagent (0-(IH-benzotriazol-1-yl)-N,N,N,N-tetramethylisourea phosphorus hexafluoride, 33.48 mg, 0.088 mmol) was dissolved in N N-dimethylformamide (1 mL), and N, N-diisopropylethylamine (0.019 mL, 0.118 mmol) was added. The reaction solution was stirred at room temperature for 1 hour. The reaction solution was directly separated by reversed-phase preparative chromatography to obtain 3-a (76 mg, 0.051 mmol, 86.36%).

Synthesis of Compound 3

[0365] Compound 3-a (76 mg, 0.051 mmol) was dissolved in dichloromethane (1.0 mL), and trifluoroacetic acid (1.0 mL) was added. The reaction solution was stirred at room temperature for 16 hours. The reaction solution was concentrated under reduced pressure and the residue was separated by reversed-phase preparative chromatography (column xBridge C18, 19*150 mm*5 um; mobile phase: water (0.1% trifluoroacetic acid), methanol; gradient: 65%-80% (initial mobile phase was 35% water/65% methanol, and ending mobile phase was 20% water/80% methanol, wherein % refers to volume percentage); 13 min; flow rate 15 mL/min) to obtain 3 (37 mg, yield: 57.26%). LC-MS (ESI): m/z=925.72(M+H).sup.+;

[0366] .sup.1H-NMR (400 MHz, D.sub.2O) : 7.45 (s, 1H), 7.27-6.18 (m, 11H), 4.3-2.25 (m, 32H), 2.22-0.60 (m, 10H).

Embodiment 4

(2S)-1-({4-[(1E)-2-(2-Methyl-3-phenylphenyl)vinyl]-5-(trifluoromethyl)-2-{[4-({2-[4,7,10-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecan-1-yl]acetyl}amino)butyl]oxy}phenyl}methyl)hexahydropyridine-2-carboxylic acid (Compound 4)

##STR00126##

Synthesis of Compound 4-c

[0367] Compound 2-c (275.82 mg, 0.5 mmol) and 1,4-diodobutane (619.84 mg, 2.000 mmol) were dissolved in N, N-dimethylformamide (2 mL), and potassium carbonate (138.21 mg, 1.00 mmol) was added, and the reaction solution was stirred at room temperature for 1 hour. The reaction solution was diluted with ethyl acetate (50 mL), and washed sequentially with water (20 mL2) and saturated brine (20 mL1). The organic phase was separated, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was separated by column chromatography (petroleum ether:ethyl acetate=20:1) to obtain product 4-c (310 mg, yield: 84.51% w).

Synthesis of Compound 4-b

[0368] Compound 4-c (410 mg, 0.559 mmol) was dissolved in ammonia-methanol solution (7 M, 11.975 mL), and the mixture was sealed in a microwave tube, and the reaction solution was stirred at 50 C. for 16 hours. The reaction solution was cooled to room temperature, concentrated under reduced pressure, and the residue was dissolved in dichloromethane (20 mL) and methanol (2 mL), and washed with 10% potassium carbonate solution (5 mL). The organic phase was separated, dried over anhydrous sodium sulfate, and filtered to obtain yellow oil 4-b (280 mg, yield: 80.45%), which was used directly in the next step without purification.

Synthesis of Compound 4-a

[0369] Compound 4-b (180 mg, 0.289 mmol), 2-(4,7,10-tris(2-(tert-butoxy)-2-oxoethyl)-1,4,7,10-tetraazacyclododecan-1-yl) acetate (198.65 mg, 0.347 mmol), HBTU reagent (0-(IH-benzotriazol-1-yl)-N,N,N,N-tetramethylisourea phosphorus hexafluoride, 164.42 mg, 0.434 mmol) was dissolved in N, N-dimethylformamide (2 mL). N, N-Diisopropylethylamine (0.096 mL, 0.578 mmol) was added. The reaction solution was stirred at room temperature for 0.5 hour, and directly separated by reversed-phase preparative chromatography (column xBridge C18, 19*150 mm*5 um; mobile phase: water (0.1% trifluoroacetic acid), methanol; gradient: 65%-80% (initial mobile phase was 35% water/65% methanol, and ending mobile phase was 20% water/80% methanol, wherein % refers to volume percentage); 13 min; flow rate 15 mL/min) to obtain 4-a (268 mg, 0.176 mmol, yield: 61.03%). LC-MS (ESI): m/z=1178.18(M+H).sup.+.

Synthesis of Compound 4

[0370] Compound 4-a (268 mg, 0.176 mmol) was dissolved in dichloromethane (2 mL), and trifluoroacetic acid (2 mL) was added. The reaction solution was stirred at room temperature for 16 hours. The reaction solution was concentrated under reduced pressure, and the residue was separated by reversed-phase preparative chromatography (column xBridge C18, 19*150 mm*5 um; mobile phase: water (0.1% trifluoroacetic acid), methanol; gradient: 65%-80% (initial mobile phase was 35% water/65% methanol, and ending mobile phase was 20% water/80% methanol, wherein % refers to volume percentage); 13 min; flow rate 15 mL/min) to obtain 4 (156 mg, yield: 68.44%). LC-MS (ESI): m/z=953.64(M+H).sup.+.

[0371] .sup.1H-NMR (400 MHz, D.sub.2O) : 7.48 (s, 1H), 7.19-6.19 (m, 11H), 4.41-2.32 (m, 33H), 2.19-0.83 (m, 13H).

Embodiment 5

##STR00127##

[0372] Compound 4 (56 mg, 0.043 mmol) and lutetium trichloride (60.82 mg, 0.216 mmol) were dissolved in sodium acetate-acetic acid buffer (pH=4.5) (2.0 mL), and the reaction solution was stirred at 90 C. for 0.5 hour. The reaction solution was cooled to room temperature and purified by pre-HPLC to obtain 5 (33 mg, yield: 52.03%). LC-MS (ESI): m/z=1125.95(M+H).sup.+.

Embodiment 6

##STR00128##

[0373] Compound 2 (182.40 mg, 0.2 mmol) and lutetium trichloride (56.26 mg, 0.200 mmol) were dissolved in sodium acetate-acetic acid buffer (pH=4.5) (2.0 mL), and the reaction solution was stirred at room temperature for 1 hour. The reaction solution was purified by pre-HPLC to obtain 6 (80 mg, 0.074 mmol, 36.90%).

[0374] LC-MS (ESI): m/z=1084.68(M+H).sup.+;

[0375] .sup.1H-NMR (400 MHz, MeOD) : 7.85 (s, 1H), 7.62 (d, J=16.0 Hz, 1H), 7.58-7.46 (m, 2H), 7.46-7.38 (m, 2H), 7.38-7.21 (m, 5H), 7.17 (d, J=7.4 Hz, 1H), 4.66-1.40 (m, 44H).

Embodiment 7

##STR00129##

[0376] Compound 2 and gallium trichloride (3.52 mg, 0.020 mmol) were dissolved in water (0.2 mL), and the reaction solution was stirred at 90 C. for 5 minutes. The reaction solution was purified directly by prep-HPLC (column XT C18, 19*150 mm*5 um; mobile phase: water (0.1% FA), acetonitrile; gradient: 25%-95% (initial mobile phase was 75% water: 25% acetonitrile, and ending mobile phase was 5% water/95% acetonitrile, wherein % refers to volume percentage); 10 min; flow rate 15 mL/min) to obtain white solid 7 (9.7 mg, yield: 99.08%).

[0377] LC-MS (ESI): m/z=978.61 (M+H).sup.+.

[0378] .sup.1H-NMR (400 MHz, MeOD) : 7.88 (s, 1H), 7.63 (d, J=15.9 Hz, 1H), 7.58-7.51 (m, 2H), 7.47-7.39 (m, 2H), 7.38-7.24 (m, 5H), 7.18 (d, J=7.5 Hz, 1H), 4.62 (d, J=13.0 Hz, 1H), 4.50-4.42 (m, 2H), 4.40 (d, J=13.1 Hz, 1H), 4.06-3.86 (m, 6H), 3.85-3.45 (m, 10H), 3.44-3.32 (m, 9H), 3.26-3.10 (m, 5H), 3.09-2.97 (m, 1H), 2.30 (s, 3H), 2.28-2.17 (m, 1H), 2.05-1.68 (m, 4H), 1.66-1.52 (m, 1H).

Embodiment 8

##STR00130##

[0379] Compound 4 (12.95 mg, 0.010 mmol), gallium trichloride (3.52 mg, 0.020 mmol) and sodium acetate (0.150 mL, 0.030 mmol) were dissolved in water (0.5 mL), and the reaction solution was stirred at 90 C. for 10 minutes. The reaction solution was cooled to room temperature, and the reaction solution was concentrated under reduced pressure, and the residue was separated by silica gel column chromatography to obtain 8 (8.76 mg, yield: 85.90%). LC-MS (ESI): m/z=1019.65 (M+H).sup.+;

[0380] .sup.1H-NMR (400 MHz, MeOD) : 7.91 (s, 1H), 7.62 (d, J=15.9 Hz, 1H), 7.57-7.49 (m, 2H), 7.46-7.38 (m, 2H), 7.38-7.23 (m, 5H), 7.18 (d, J=6.8 Hz, 1H), 4.52 (dd, J=34.7, 12.7 Hz, 2H), 4.37-4.22 (m, 2H), 3.89-3.46 (m, 13H), 3.45-2.96 (m, 16H), 2.30 (s, 3H), 2.28-2.19 (m, 1H), 2.05-1.90 (m, 3H), 1.89-1.67 (m, 5H), 1.66-1.50 (m, 1H).

Embodiment 9

##STR00131##

Synthesis of Compound 9-d

[0381] 2-Methylpropan-2-yl (2S)-1-[(2-{[2-(1,3-dioxo-2,3-dihydro-1H-isoindole-2-yl)ethyl]oxy}-4-[(1E)-2-(2-methyl-3-phenylphenyl)vinyl]-5-(trifluoromethyl)phenyl)methyl]hexahydropyridine-2-carboxylate (610 mg, 0.842 mmol) and hydrazine hydrate (0.511 mL, 8.416 mmol) were dissolved in methanol (6 mL). The reaction solution was stirred at 60 C. for 2 hours. The reaction solution was cooled to room temperature, and concentrated under reduced pressure, and the residue was washed with dichloromethane (6 mL), filtered, and the filtrate was concentrated under reduced pressure to obtain 9-d (498 mg, yield: 99.50%). LC-MS (ESI): m/z=595.53(M+H).sup.+.

Synthesis of Compound 9-c

[0382] N, N-Diisopropylethylamine (0.020 mL, 0.120 mmol), compound 9-d (59.47 mg, 0.1 mmol), (1r,4r)-4-(((((9H-fluoren-9-yl)methoxy)carbonyl)amino)methyl)cyclohexane-1-carboxylic acid (37.95 mg, 0.100 mmol), and benzotriazole-N,N,N,N-tetramethyluronium hexafluorophosphate (45.51 mg, 0.120 mmol) were dissolved in N, N-dimethylformamide (0.5 mL), and the reaction solution was stirred at room temperature for 30 minutes. The reaction solution was diluted with ethyl acetate (20 mL), and washed sequentially with water (20 mL2) and saturated brine (10 mL1). The organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (petroleum ether:ethyl acetate:ethanol=20:10:1) to obtain 9-c (72 mg, yield: 75.30%).

Synthesis of Compound 9-b

[0383] Piperidine (0.021 mL, 0.226 mmol) and compound 9-c (72 mg, 0.075 mmol) were dissolved in acetonitrile (1 mL). The reaction solution was stirred at room temperature for 5 hours. The reaction solution was concentrated under reduced pressure, and the residue was separated by silica gel column chromatography (dichloromethane:methanol:ammonia methanol=400:100:1) to obtain 9-b (49 mg, yield: 88.66%).

Synthesis of Compound 9-a

[0384] N, N-Diisopropylethylamine (0.017 mL, 0.100 mmol), compound 9-b (49 mg, 0.067 mmol), (10-{1-[(2-methylpropan-2-yl)oxy]-1-oxoethyl-2-yl}-4,7-bis{2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl}-1,4,7,10-tetraazacyclododecan-1-yl)acetic acid (42.06 mg, 0.073 mmol), and benzotriazole-N,N,N,N-tetramethyluronium hexafluorophosphate (32.92 mg, 0.087 mmol) were dissolved in N, N-dimethylformamide (0.5 mL), and the reaction solution was stirred at room temperature for 1 hour, and the residue was separated by Prep-HPLC to obtain 9-a (72 mg, yield: 83.39%).

Synthesis of Compound 9

[0385] Trifluoroacetic acid (2.0 mL) and compound 9-a (72 mg, 0.056 mmol) were dissolved in dichloromethane (2.0 mL), and the reaction solution was stirred at room temperature for 16 hours. The reaction solution was concentrated under reduced pressure, and the residue was separated by Prep-HPLC to obtain 9 (59.46 mg, yield: 67.27%). LC-MS (ESI): m/z=1065.21 (M+H).sup.+.

Embodiment 10

##STR00132##

Synthesis of Compound 10-d

[0386] 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (191.70 mg, 1.000 mmol), 4-(4-methylphenyl) butyric acid (178.23 mg, 1.00 mmol) and 1-hydroxytetrahydro-1H-pyrrole-2,5-dione (115.09 mg, 1.000 mmol) were dissolved in dimethyl sulfoxide (2 mL). The reaction was stirred at room temperature for 48 hours. (2S)-6-Amino-2-({[(9H-fluoren-9-ylmethyl)oxy]carbonyl}amino)hexanoic acid (368.43 mg, 1.000 mmol) was added, and the reaction solution was continuously stirred at room temperature for 1 hour. The reaction solution was directly separated by Prep-HPLC to obtain 10-d (400 mg, yield: 75.66%).

Synthesis of Compound 10-c

[0387] 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (188.56 mg, 0.984 mmol), compound 10-d and 1-hydroxytetrahydro-1H-pyrrole-2,5-dione (95.79 mg, 0.832 mmol) were dissolved in dimethyl sulfoxide (2 mL). The reaction solution was stirred at room temperature for 2 hours. The reaction solution was directly separated by Prep-HPLC to obtain 10-c (400 mg, yield: 84.49%).

Synthesis of Compound 10-b

[0388] Compound 9-d (59.47 mg, 0.1 mmol) and compound 10-c (75.09 mg, 0.120 mmol) were dissolved in acetonitrile (1 mL). The reaction solution was stirred at room temperature for 1 hour. Piperidine (0.037 mL, 0.400 mmol) was added, and the reaction solution was continuously stirred at room temperature for 2 hours. The reaction solution was concentrated under reduced pressure, and the residue was separated by silica gel column chromatography (petroleum ether:ethyl acetate=5:1, 6 CV, then dichloromethane:methanol=10:1, 8 CV, CV is the column volume) to obtain 10-b (78 mg, yield: 88.32%).

Synthesis of Compound 10-a

[0389] N, N-Diisopropylethylamine (0.029 mL, 0.177 mmol), compound 10-b (78 mg, 0.088 mmol), (10-{1-[(2-methylpropan-2-yl)oxy]-1-oxoethyl-2-yl}-4,7-bis{2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl}-1,4,7,10-tetraazacyclododecan-1-yl)acetic acid (55.65 mg, 0.097 mmol), and benzotriazole-N,N,N,N-tetramethyluronium hexafluorophosphate (43.54 mg, 0.115 mmol) were dissolved in N, N-dimethylformamide (1.0 mL), and the reaction solution was stirred at room temperature for 1 hour, and directly separated by Prep-HPLC to obtain 10-a (108 mg, yield: 85.04%).

Synthesis of Compound 10

[0390] Trifluoroacetic acid (2.0 mL) and compound 10-a (72 mg, 0.056 mmol) were dissolved in dichloromethane (2.0 mL), and the reaction solution was stirred at room temperature for 16 hours. The reaction solution was concentrated under reduced pressure, and the residue was separated by Prep-HPLC to obtain 10 (50 mg, yield: 54.86%). LC-MS (ESI): m/z=1214.47 (M+H).sup.+.

Embodiment 11

##STR00133## ##STR00134##

Synthesis of Compound 11-b

[0391] Compound 4-b (124.55 mg, 0.20 mmol) and compound 10-c (150.17 mg, 0.240 mmol) were dissolved in acetonitrile (5.0 mL). The reaction solution was stirred at room temperature for 1 hour, and dichloromethane (2.0 mL) was added and the reaction solution was stirred for 1 hour. Piperidine (0.073 mL, 0.800 mmol) was added, and the reaction solution was continuously stirred at room temperature for 2 hours. The reaction solution was concentrated under reduced pressure, and the residue was separated by silica gel column chromatography (petroleum ether:ethyl acetate=5:1) to obtain 11-b (177 mg, yield: 97.13%).

Synthesis of Compound 11-a

[0392] N, N-Diisopropylethylamine (0.064 mL, 0.389 mmol), 11-b (78 mg, 0.088 mmol), (10-{1-[(2-methylpropan-2-yl)oxy]-1-oxoethyl-2-yl}-4,7-bis{2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl}-1,4,7,10-tetraazacyclododecan-1-yl)acetic acid (122.39 mg, 0.214 mmol) and benzotriazole-N,N,N,N-tetramethyluronium hexafluorophosphate (95.77 mg, 0.253 mmol) were dissolved in N, N-dimethylformamide (2.0 mL), and the reaction solution was stirred at room temperature for 1 hour. The reaction solution was concentrated under reduced pressure, and the residue was separated by silica gel column chromatography (ethyl acetate, 6 CV, then dichloromethane:methanol=10:1, 8 CV, CV is column volume) to obtain 11-a (284 mg, yield: 99.73%).

Synthesis of Compound 11

[0393] Compound 11-a (284 mg, 0.194 mmol) was dissolved in dichloromethane (3 mL), and the reaction solution was cooled to 0 C., and trifluoroacetic acid (3 mL) was added. The reaction solution was stirred at room temperature for 16 hours. The reaction solution was concentrated under reduced pressure, and the residue was purified by reversed-phase preparative chromatography to obtain 11 (150 mg, 0.121 mmol, 62.37%).

[0394] .sup.1H-NMR (400 MHz, MeOD) : 8.00 (s, OH), 7.80 (s, 1H), 7.52 (d, J=15.8 Hz, 1H), 7.47-7.40 (m, 2H), 7.36-7.29 (m, 2H), 7.28-7.15 (m, 5H), 7.08 (d, J=7.0 Hz, 1H), 6.94 (s, 4H), 4.48 (d, J=12.7 Hz, 1H), 4.33 (d, J=12.9 Hz, 1H), 4.23-4.13 (m, 3H), 3.75-3.59 (m, 5H), 3.56-3.26 (m, 11H), 3.10-2.87 (m, 11H), 2.50-2.41 (m, 2H), 2.20 (s, 3H), 2.16 (s, 3H), 2.11-2.05 (m, 2H), 1.96-1.16 (m, 22H).

Embodiment 12

##STR00135##

Synthesis of Compound 12

[0395] Compound 11 (30 mg, 0.024 mmol) and lutetium trichloride (13.60 mg, 0.048 mmol) were dissolved in methanol (1.0 mL) and sodium acetate-acetic acid buffer (pH=4.5) (0.5 mL). The reaction solution was stirred at room temperature for 20 minutes, then stirred at 90 C. for 5 minutes, and the reaction solution was cooled to room temperature. The reaction solution was directly separated by reversed-phase Pre-HPLC to obtain 12 (14 mg, yield: 48.08%). LC-MS (ESI): m/z=1414.3 (M+H).sup.+.

Embodiment 13

##STR00136##

Synthesis of Compound 13

[0396] Compound 10 (12.13 mg, 0.01 mmol) and lutetium trichloride (5.63 mg, 0.020 mmol) were dissolved in sodium acetate-acetic acid buffer (pH=4.5) (1.0 mL). The reaction solution was stirred at room temperature for 20 minutes, then stirred at 90 C. for 5 minutes, and the reaction solution was cooled to room temperature. The reaction solution was directly separated by reversed-phase Pre-HPLC to obtain 13 (10 mg, yield: 72.20%). LC-MS (ESI): m/z=1386.7 (M+H).sup.+.

Embodiment 14

##STR00137##

Synthesis of Compound 14

[0397] Compound 9 (10.64 mg, 0.01 mmol) and lutetium trichloride (5.63 mg, 0.020 mmol) were dissolved in sodium acetate-acetic acid buffer (pH=4.5) (1.0 mL). The reaction solution was stirred at room temperature for 20 minutes, then the reaction solution was stirred at 90 C. for 5 minutes, and the reaction solution was cooled to room temperature. The reaction solution was directly separated by reversed-phase Pre-HPLC to obtain 14 (6 mg, yield: 48.54%). LC-MS (ESI): m/z=1237.3 (M+H).sup.+.

Embodiment 15

##STR00138##

Synthesis of Compound 15

[0398] Compound 1 (15 mg, 0.017 mmol) and lutetium trichloride (23.89 mg, 0.085 mmol) were dissolved in sodium acetate-acetic acid buffer (pH=4.5) (1.0 mL), and the reaction solution was stirred at room temperature for 1 hour. The reaction solution was directly separated by Prep-HPLC to obtain 15 (8.6 mg, yield: 36%). LC-MS (ESI): m/z=1055.79(M+H).sup.+.

[0399] .sup.1H-NMR (400 MHz, D.sub.2O) : 7.20 (s, 1H), 7.15-6.87 (m, 6H), 6.81 (s, 1H), 6.75-6.22 (m, 4H), 4.50-3.82 (m, 3H), 3.78-2.89 (m, 17H), 2.86-2.18 (m, 13H), 2.08-0.96 (m, 9H).

Embodiment 16

##STR00139## ##STR00140##

Synthesis of Compound 16-c

[0400] Compound 2-c (500 mg, 0.910 mmol) was dissolved in N, N-dimethylformamide (15 mL), and 1,5-diiodopentane (294.66 mg, 0.910 mmol) and potassium carbonate (314.30 mg, 2.274 mmol) were added, and the reaction solution was stirred at room temperature for 2 hours. The reaction solution was diluted with ethyl acetate (50 mL), and washed sequentially with water (20 mL2) and saturated brine (20 mL1). The organic phase was separated, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was separated by column chromatography to obtain 16-c (171 mg, yield: 25.20%).

Synthesis of Compound 16-b

[0401] Compound 16-c (171 mg, 0.229 mmol) was dissolved in tetrahydrofuran (2 mL), and ammonia methanol solution (7 M, 10 mL) was added. The reaction solution was stirred at 50 C. for 12 hours. The reaction solution was cooled to room temperature, and the reaction solution was diluted with ethyl acetate (5 mL), and washed sequentially with water (2 mL2) and saturated brine (2 mL1). The organic phase was separated, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain 16-b (145 mg, yield: 99.61%).

Synthesis of Compound 16-a

[0402] Compound 16-b (145 mg, 0.228 mmol) was dissolved in N, N-dimethylformamide (5 mL), and [4,7,10-tris(4,4-dimethyl-2-oxopentyl)-1,4,7,10-tetraazacyclododecan-1-yl]acetic acid (155.36 mg, 0.274 mmol), benzotriazole-N,N,N,N-tetramethyluronium hexafluorophosphate (129.70 mg, 0.342 mmol), and N, N-diisopropylethylamine (0.075 mL, 0.456 mmol) were added. The reaction solution was stirred at room temperature for 1 hour, then the reaction solution was diluted with ethyl acetate (5 mL), and washed sequentially with water (2 mL2) and saturated brine (2 mL1). The organic phase was separated, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain 16-a (243 mg, yield: 98.10%).

Synthesis of Compound 16

[0403] Compound 16-a (243 mg, 0.224 mmol) was dissolved in dichloromethane (10 mL), and trifluoroacetic acid (10 mL) was added. The reaction solution was stirred at room temperature for 18 hours, and the reaction solution was concentrated under reduced pressure, and the residue was directly separated by prep-HPLC to obtain 16 (104.77 mg, yield: 48.35%). LC-MS (ESI): m/z=968.4 (M+H).sup.+.

Embodiment 17

##STR00141##

Synthesis of Compound 17

[0404] Compound 16 (49 mg, 0.051 mmol) was dissolved in sodium acetate-acetic acid buffer (pH=4.5) (10 mL), and lutetium trichloride (28.69 mg, 0.102 mmol) was added. The reaction solution was stirred at room temperature for 10 minutes, and directly separated by prep-HPLC to obtain 17 (29.67 mg, yield: 51.41%). LC-MS (ESI): m/z=1140.7 (M+H).sup.+.

Embodiment 18

##STR00142## ##STR00143##

Synthesis of Compound 18-c

[0405] 1-{[(9H-Fluoren-9-ylmethyl)oxy]carbonyl}hexahydropyridine-4-carboxylic acid (702.80 mg, 2.00 mmol), 1-hydroxytetrahydro-1H-pyrrole-2,5-dione (230.18 mg, 2.000 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (383.40 mg, 2.000 mmol) were dissolved in acetonitrile (7.0 mL) and dichloromethane (7.0 mL), and the reaction solution was stirred at room temperature for 5 hours, and directly separated by reversed-phase chromatography to obtain 18-c (800 mg, yield: 89.19%).

Synthesis of Compound 18-b

[0406] Compound 9-d (59.47 mg, 0.100 mmol) and compound 18-c (57.41 mg, 0.128 mmol) were dissolved in acetonitrile (1.0 mL), and the reaction solution was stirred at room temperature for 16 hours. Piperidine (85.15 mg, 1.000 mmol) was added, and the stirring was continued for 1 hour, and the reaction solution was concentrated under reduced pressure, and the residue was purified by silica gel column (petroleum ether:ethyl acetate=5:1, 6 CV, dichloromethane:methanol=7:3, 6 CV) to obtain 18-b (50 mg, yield: 70.83%).

Synthesis of Compound 18-a

[0407] N, N-Diisopropylethylamine (0.023 mL, 0.142 mmol), compound 18-b (50 mg, 0.071 mmol), (10-{1-[(2-methylpropan-2-yl)oxy]-1-oxoethyl-2-yl}-4,7-bis{2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl}-1,4,7,10-tetraazacyclododecan-1-yl)acetic acid (44.63 mg, 0.078 mmol), and O-benzotriazole-tetramethyluronium hexafluorophosphate (34.92 mg, 0.092 mmol) were dissolved in N, N-dimethylformamide (1.0 mL), and the reaction solution was stirred at room temperature for 1 hour, then directly purified by silica gel column (petroleum ether:ethyl acetate=5:1, 6 CV, dichloromethane:methanol=10:1, 6 CV, CV is column volume) to obtain 18-a (80 mg, yield: 89.59%).

Synthesis of Compound 18

[0408] Compound 18-a (80 mg, 0.063 mmol) was dissolved in dichloromethane (2.0 mL), and trifluoroacetic acid (2.0 mL) was added. The reaction solution was stirred at room temperature for 24 hours, and the reaction solution was concentrated under reduced pressure to obtain compound 18 (30 mg, yield: 45.62%). LC-MS (ESI): m/z=1037.3 (M+H).sup.+.

Embodiment 19

##STR00144## ##STR00145##

Synthesis of Compound 19-b

[0409] Compound 19-c (284 mg, 0.379 mmol) was dissolved in tetrahydrofuran (2 mL) and hydrochloric acid in 1,4-dioxane (4 M in dioxane) (1.5 mL) was added. The reaction solution was stirred at room temperature for 5 hours. The reaction solution was quenched with potassium carbonate aqueous solution (20% aqueous, 5 mL). The mixture was extracted with dichloromethane (20 mL2), and the organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain 19-b (246 mg, yield: 99.990%), which was directly carried out in the next step of reaction without purification.

Synthesis of Compound 19-a

[0410] Compound 19-b (246 mg, 0.379 mmol), (10-{1-[(2-methylpropan-2-yl)oxy]-1-oxoethyl-2-yl}-4,7-bis{2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl}-1,4,7,10-tetraazacyclododecan-1-yl)acetic acid (238.87 mg, 0.417 mmol), and benzotriazole-N,N,N,N-tetramethyluronium hexafluorophosphate (186.93 mg, 0.493 mmol) were dissolved in N, N-dimethylformamide (2.0 mL), and N, N-diisopropylethylamine (0.125 mL, 0.758 mmol) was added. The reaction solution was stirred at room temperature for 1 hour. The reaction solution was concentrated under reduced pressure, and the residue was separated by silica gel column chromatography (petroleum ether:ethyl acetate:ethanol=10:20:1) to obtain 19-a (360 mg, yield: 78.89%).

Synthesis of Compound 19

[0411] Compound 19-a (360 mg, 0.299 mmol) was dissolved in dichloromethane (3 mL), and trifluoroacetic acid (3 mL) was added. The reaction solution was stirred at room temperature for 16 hours, and the reaction solution was concentrated under reduced pressure, and the residue was directly separated by pre-HPLC to obtain 19 (194 mg, yield: 66.24%). LC-MS (ESI): m/z=980.7 (M+H).sup.+.

Embodiment 20

##STR00146##

Synthesis of Compound 20

[0412] Compound 19 (23.50 mg, 0.024 mmol) and lutetium trichloride (13.50 mg, 0.048 mmol) were dissolved in sodium acetate-acetic acid buffer (pH=4.5) (1 mL), and the reaction solution was stirred at 90 C. for 5 minutes. The reaction solution was cooled to room temperature, and directly separated by pre-HPLC to obtain 20 (23 mg, yield: 83.24%). LC-MS (ESI): m/z=1152.1 (M+H).sup.+.

Embodiment 21

##STR00147## ##STR00148## ##STR00149## ##STR00150##

Synthesis of Compound 21-f

[0413] 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (383.40 mg, 2.000 mmol), 4-(4-methylphenyl) butyric acid (356.46 mg, 2.00 mmol), and 1-hydroxytetrahydro-1H-pyrrole-2,5-dione (230.18 mg, 2.000 mmol) were added to dimethyl sulfoxide (4 mL). The reaction was stirred at room temperature for 48 hours. (2S)-6-Amino-2-({[(9H-fluoren-9-ylmethyl)oxy]carbonyl}amino)hexanoic acid (736.86 mg, 2.00 mmol) was added, and the reaction solution was continuously stirred at room temperature for 1 hour. The reaction solution was directly separated by reversed-phase chromatography (120 g of C.sub.18, water (0.1% formic acid), 0-95% acetonitrile, 6 CV, CV is column volume) to obtain 21-f (860 mg, yield: 81.34%).

Synthesis of Compound 21-e

[0414] 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (498.97 mg, 2.603 mmol), compound 21-f (860 mg, 1.627 mmol) and 1-hydroxytetrahydro-1H-pyrrole-2,5-dione (252.76 mg, 2.196 mmol) were added to dimethyl sulfoxide (2 mL). The reaction solution was stirred at room temperature for 2 hours. The reaction solution was directly separated by reversed-phase chromatography (120 g of C.sub.18, water (0.1% formic acid), 0-95% acetonitrile, 6 CV, CV is column volume) to obtain 21-e (900 mg, yield: 88.42%).

Synthesis of Compound 21-d

[0415] N, N-Diisopropylethylamine (0.040 mL, 0.240 mmol), compound 9-d (118.94 mg, 0.20 mmol), (1r,4r)-4-(((((9H-fluoren-9-yl)methoxy)carbonyl)amino)methyl)cyclohexane-1-carboxylic acid (75.89 mg, 0.200 mmol), and benzotriazole-N,N,N,N-tetramethyluronium hexafluorophosphate (91.02 mg, 0.240 mmol) were dissolved in N, N-dimethylformamide (1.0 mL). The reaction was stirred at room temperature for 30 minutes. The reaction solution was diluted with ethyl acetate (20 mL), and washed sequentially with water (20 mL2) and saturated brine (10 mL1). The organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was separated by silica gel column chromatography (petroleum ether:ethyl acetate:ethanol=20:10:1) to obtain 21-d (164 mg, yield: 85.76%).

Synthesis of Compound 21-c

[0416] Piperidine (0.047 mL, 0.515 mmol) and compound 21-d (164 mg, 0.172 mmol) were dissolved in acetonitrile (2 mL). The reaction solution was stirred at room temperature for 2 hours. The reaction solution was concentrated under reduced pressure, and the residue was separated by silica gel column (dichloromethane:methanol:ammonia methanol (7 M in MeOH)=400:100:1) to obtain 21-c (110 mg, yield: 87.38%).

Synthesis of Compound 21-b

[0417] Compound 21-c (110 mg, 0.150 mmol) and compound 21-e (112.63 mg, 0.180 mmol) were dissolved in acetonitrile (2 mL). The reaction solution was stirred at room temperature for 1 hour, and dichloromethane (2.0 mL) was added to continue stirring for 1 hour. Piperidine (0.069 mL, 0.749 mmol) was added, and the reaction solution was continuously stirred at room temperature for 2 hours. The reaction solution was concentrated under reduced pressure, and the residue was separated by silica gel column chromatography (petroleum ether:ethyl acetate=5:1, then, dichloromethane:methanol:ammonia methanol (7 M in MeOH)=100:10:2) to obtain 21-b (127 mg, yield: 82.82%).

Synthesis of Compound 21-a

[0418] Compound 21-b (127 mg, 0.124 mmol), (4,7,10-tris{2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl}-1,4,7,10-tetraazacyclododecan-1-yl)acetic acid (92.33 mg, 0.161 mmol) and O-benzotriazole-tetramethyluronium hexafluorophosphate (70.54 mg, 0.186 mmol) were dissolved in N, N-dimethylformamide (1.0 mL), and N, N-diisopropylethylamine (0.041 mL, 0.248 mmol) was added. The reaction solution was stirred at room temperature for 1 hour, and the reaction solution was concentrated under reduced pressure, and the residue was separated by silica gel column (petroleum ether:ethyl acetate=4:1, 6 CV, then 100% PE, 5 CV, then dichloromethane:methanol=10:1, 8 CV, CV is column volume) to obtain 21-a (195 mg, yield: 99.54%).

Synthesis of Compound 21

[0419] Compound 21-b (195 mg, 0.124 mmol) was dissolved in dichloromethane (2 mL), and trifluoroacetic acid (2 mL) was added. The reaction solution was stirred at room temperature for 16 hours, and the reaction solution was concentrated under reduced pressure, and directly separated by pre-HPLC to obtain 21 (100 mg, yield: 59.79%). LC-MS (ESI): m/z=1353.61 (M+H).sup.+.

Embodiment 22

##STR00151##

Synthesis of Compound 22

[0420] Compound 21 (13.53 mg, 0.01 mmol) was dissolved in sodium acetate-acetic acid buffer (pH=4.5) (1 mL), and lutetium trichloride (5.63 mg, 0.020 mmol) was added, and the reaction solution was heated and stirred at 90 C. for 10 minutes. The reaction solution was directly separated by Prep-HPLC to obtain 22 (10 mg, yield: 65.59%). LC-MS (ESI): m/z=1525.55 (M+H).sup.+.

Embodiment 23

##STR00152## ##STR00153##

Synthesis of Compound 23-c

[0421] Compound 2-c (500 mg, 0.910 mmol) was dissolved in N, N-dimethylformamide (15 mL), and 1,6-diiodohexane (307.55 mg, 0.910 mmol) and potassium carbonate (314.43 mg, 2.275 mmol) were added, and the reaction solution was stirred at room temperature for 2 hours. The reaction solution was diluted with ethyl acetate (50 mL), and washed sequentially with water (20 mL2) and saturated saline (20 mL1). The organic phase was separated, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was separated by column chromatography to obtain 23-c (462 mg, yield: 66.82%).

Synthesis of Compound 23-b

[0422] Compound 23-c (462 mg, 0.608 mmol) was dissolved in tetrahydrofuran (2 mL), and ammonia methanol solution (7 M, 15 mL) was added. The reaction solution was stirred at 50 C. for 16 hours. The reaction solution was cooled to room temperature, and the reaction solution was diluted with ethyl acetate (5 mL), and washed sequentially with water (2 mL2) and saturated saline (2 mL1). The organic phase was separated, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain crude product 23-b (483 mg, yield: 122.41%), which was directly carried out in the next step of reaction without purification.

Synthesis of Compound 23-a

[0423] Compound 23-b (145 mg, 0.228 mmol) was dissolved in N, N-dimethylformamide (5 mL), and [4,7,10-tris(4,4-dimethyl-2-oxopentyl)-1,4,7,10-tetraazacyclododecan-1-yl]acetic acid (104.83 mg, 0.185 mmol), benzotriazole-N,N,N, N-tetramethyluronium hexafluorophosphate (87.67 mg, 0.231 mmol), and N, N-diisopropylethylamine (0.051 mL, 0.308 mmol) were added. The reaction solution was stirred at room temperature for 1 hour, and the reaction solution was diluted with ethyl acetate (5 mL) and washed sequentially with water (2 mL2) and saturated brine (2 mL1). The organic phase was separated, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain 23-a (91 mg, yield: 49.10%).

Synthesis of Compound 23

[0424] Compound 23-a (91 mg, 0.076 mmol) was dissolved in dichloromethane (10 mL), and trifluoroacetic acid (10 mL) was added. The reaction solution was stirred at room temperature for 18 hours, and the reaction solution was concentrated under reduced pressure, and the residue was directly separated by prep-HPLC to obtain 23 (55.42 mg, yield: 74.34%). LC-MS (ESI): m/z=982.12 (M+H).sup.+.

Embodiment 24

##STR00154##

Synthesis of Compound 24

[0425] Compound 23 (30 mg, 0.031 mmol) was dissolved in sodium acetate-acetic acid buffer (pH=4.5) (10 mL), and lutetium trichloride (17.20 mg, 0.061 mmol) was added. The reaction solution was stirred at room temperature for 10 minutes, and directly separated by prep-HPLC to obtain 24 (28.12 mg, yield: 78.67%). LC-MS (ESI): m/z=1154.3 (M+H).sup.+.

Embodiment 25

##STR00155## ##STR00156##

Synthesis of Compound 25-b

[0426] Compound 23-b (200 mg, 0.308 mmol) was dissolved in acetonitrile (5 mL) and dichloromethane (5 mL), and 9H-fluoren-9-ylmethyl {[(2S)-125-b-[(2,5-dioxytetrahydro-1H-pyrrole-1-yl)oxy]-6-{[4-(4-methylphenyl)-1-oxybutyl]amino}-1-oxohex-2-yl]amino}formate (231.44 mg, 0.370 mmol) was added, and the reaction solution was stirred at room temperature for 1 hour. Piperidine (0.102 mL, 0.616 mmol) was added to continue stirring for 1 hour, and the reaction solution was diluted with ethyl acetate (5 mL), and washed sequentially with water (2 mL2) and saturated brine (2 mL1). The organic phase was separated, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain 25-b (184 mg, yield: 63.69%).

Synthesis of Compound 25-a

[0427] Compound 25-b (184 mg, 0.196 mmol) was dissolved in N, N-dimethylformamide (5 mL), and (4,7,10-tris{2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl}-1,4,7,10-tetraazacyclododecan-1-yl)acetic acid (112.44 mg, 0.196 mmol), benzotriazole-N,N,N,N-tetramethyluronium hexafluorophosphate (111.68 mg, 0.294 mmol), and N, N-diisopropylethylamine (0.065 mL, 0.393 mmol) were added, and the reaction solution was stirred at room temperature for 1 hour. The reaction solution was diluted with ethyl acetate (5 mL), and washed sequentially with water (2 mL2) and saturated brine (2 mL1). The organic phase was separated, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain 25-a (158.85 mg, yield: 54.16%).

Synthesis of Compound 25

[0428] Compound 25-a (158.85 mg, 0.106 mmol) was dissolved in dichloromethane (10 mL), and trifluoroacetic acid (10 mL) was added. The reaction solution was stirred at room temperature for 18 hours, and the reaction solution was concentrated under reduced pressure, and the residue was directly separated by prep-HPLC to obtain 25 (84.5 mg, yield: 62.60%). LC-MS (ESI): m/z=1270.5 (M+H).

Embodiment 26

##STR00157##

Synthesis of Compound 26

[0429] Compound 25 (20 mg, 0.016 mmol) was dissolved in sodium acetate-acetic acid buffer (pH=4.5) (3 mL), and lutetium trichloride (8.86 mg, 0.032 mmol) was added. The reaction solution was stirred at room temperature for 10 minutes, and directly separated by prep-HPLC to obtain 26 (19.02 mg, yield: 83.75%). LC-MS (ESI): m/z=1142.46(M+H).sup.+.

Embodiment 27

##STR00158##

Synthesis of Compound 27

[0430] Compound 25 (20 mg, 0.016 mmol) was added to water (2 mL), and gallium trichloride (0.640 mL, 0.032 mmol) was added. The reaction solution was stirred at 90 C. for 10 minutes, cooled to room temperature, and directly separated by prep-HPLC to obtain 27 (17.37 mg, yield: 81.24%). LC-MS (ESI): m/z=1337.21(M+H).sup.+.

Embodiment 28

##STR00159##

Synthesis of Compound 28

[0431] Compound 23 (8 mg, 0.008 mmol) was added to water (2 mL), and sodium acetate (0.164 mL, 0.024 mmol) was added, and the reaction solution was stirred for 1 minute, and gallium trichloride (0.319 mL, 0.016 mmol) was added. The reaction solution was stirred at 90 C. for 10 minutes, and the reaction solution was cooled to room temperature, and directly separated by prep-HPLC to obtain 28 (4.92 mg, yield: 57.61%). LC-MS (ESI): m/z=1048.82(M+H).sup.+.

Embodiment 29

##STR00160##

Synthesis of Compound 29

[0432] Compound 16 (20 mg, 0.021 mmol) was added to water (2 mL), and gallium trichloride (0.809 mL, 0.041 mmol) was added. The reaction solution was stirred at 90 C. for 10 minutes, and the reaction solution was cooled to room temperature, and directly separated by prep-HPLC to obtain 29 (19.64 mg, yield: 90.47%). LC-MS (ESI): m/z=1334.8(M+H).sup.+.

Embodiment 30

##STR00161## ##STR00162## ##STR00163##

Synthesis of Compound 30-d

[0433] Compound 2-c (551.65 mg, 1.00 mmol), 2-methylpropan-2-yl ({2-[(2-bromoethyl)oxy]ethyl}amino) formate (321.78 mg, 1.200 mmol), and potassium carbonate (179.66 mg, 1.300 mmol) were dissolved in N, N-dimethylformamide (3.0 mL). The reaction solution was stirred at 80 C. for 60 hours. The reaction solution was cooled to room temperature, diluted with ethyl acetate (40 mL), and washed sequentially with water (20 mL2) and saturated brine (20 mL1). The organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was separated by silica gel column chromatography (petroleum ether:ethyl acetate=10:3) to obtain 30-d (438 mg, yield: 59.28%).

Synthesis of Compound 30-c

[0434] Compound 30-d (438 mg, 0.593 mmol) was dissolved in tetrahydrofuran (4 mL), and hydrochloric acid in 1,4-dioxane (4 M) (4 mL) was added, and the reaction solution was stirred at room temperature for 1 hour, and the reaction solution was concentrated under reduced pressure to obtain 30-c (260 mg, yield: 68.64%).

Synthesis of Compound 30-b

[0435] Compound 30-c (127.75 mg, 0.2 mmol), compound 21-e (150.17 mg, 0.240 mmol) were dissolved in acetonitrile (2.0 mL) and dichloromethane (2.0 mL). The reaction solution was stirred at room temperature for 1 hour, and piperidine (0.183 mL, 2.00 mmol) was added, and the reaction solution was continuously stirred at room temperature for 2 hours. The reaction solution was concentrated under reduced pressure, and the residue was separated by silica gel column (petroleum ether:ethyl acetate=5:1, 6 CV, then, dichloromethane:methanol:ammonia methanol (7 M in MeOH)=100:10:2, 8 CV, CV is column volume) to obtain 30-b (160 mg, yield: 86.29%).

Synthesis of Compound 30-a

[0436] N, N-Diisopropylethylamine (0.057 mL, 0.346 mmol), compound 30-b (160 mg, 0.173 mmol), (4,7,10-tris{2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl}-1,4,7,10-tetraazacyclododecan-1-yl)acetic acid (118.61 mg, 0.207 mmol), and benzotriazole-N,N,N,N-tetramethyluronium hexafluorophosphate (85.29 mg, 0.225 mmol) were dissolved in N, N-dimethylformamide (2.0 mL), and the reaction solution was stirred at room temperature for 1 hour. The reaction solution was concentrated under reduced pressure. The residue was separated by column chromatography (petroleum ether:ethyl acetate=4:1, 6 CV, then 100% PE, 5 CV, then dichloromethane:methanol=10:1, 8 CV, CV is the column volume) to obtain 30-a (255 mg, 0.172 mmol, 99.71%).

Synthesis of Compound 30

[0437] Trifluoroacetic acid (3 mL) and compound 30-a (255 mg, 0.172 mmol) were dissolved in dichloromethane (3 mL). The reaction solution was stirred at room temperature for 16 hours. The reaction solution was concentrated under reduced pressure, and the residue was separated by Pre-HPLC to obtain 30 (121 mg, yield: 55.92%). LC-MS (ESI): m/z=1258.46(M+H).sup.+.

Embodiment 31

##STR00164## ##STR00165##

Synthesis of Compound 31-a

[0438] N, N-Diisopropylethylamine (0.033 mL, 0.200 mmol), compound 30-c (63.88 mg, 0.1 mmol), (4,7,10-tris{2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl}-1,4,7,10-tetraazacyclododecan-1-yl)acetic acid (68.73 mg, 0.120 mmol) and benzotriazole-N,N,N,N-tetramethyluronium hexafluorophosphate (49.30 mg, 0.130 mmol) were dissolved in acetonitrile (1.0 mL), and the reaction solution was stirred at room temperature for 0.5 hour. The reaction solution was concentrated under reduced pressure, and the residue was separated by column chromatography (petroleum ether:ethyl acetate=5:1, then, dichloromethane:methanol:ammonia methanol (7 M in MeOH)=200:20:1) to obtain 31-a (119 mg, yield: 99.71%).

Synthesis of Compound 31

[0439] Trifluoroacetic acid (2.0 mL) and compound 31-a (119 mg, 0.100 mmol) were dissolved in dichloromethane (2.0 mL). The reaction solution was reacted at room temperature for 16 hours. The reaction solution was concentrated under reduced pressure, and the residue was separated by Pre-HPLC to obtain 31 (47 mg, yield: 48.64%). LC-MS (ESI): m/z=970.13(M+H).sup.+.

Embodiment 32

##STR00166##

Synthesis of Compound 32

[0440] Compound 30 (12.57 mg, 0.01 mmol) and lutetium trichloride (5.63 mg, 0.020 mmol) were added to sodium acetate-acetic acid buffer (pH=4.5) (1.0 mL), and the reaction solution was stirred at 90 C. for 10 minutes. The reaction solution was cooled to room temperature, and directly separated by reversed-phase chromatography to obtain 32 (7.2 mg, yield: 50.38%). LC-MS (ESI): m/z=1430.4(M+H).sup.+.

Embodiment 33

##STR00167##

Synthesis of Compound 33

[0441] Lutetium trichloride (5.63 mg, 0.020 mmol) and compound 31 (9.69 mg, 0.01 mmol) were added to sodium acetate-acetic acid buffer (pH=4.5) (1.0 mL), and the reaction solution was stirred at 90 C. for 5 minutes, and the reaction solution was cooled to room temperature. The reaction solution was directly separated by Pre-HPLC to obtain 33 (8.7 mg yield: 76.25%). LC-MS (ESI): m/z=1142.01(M+H).sup.+.

Embodiment 34

##STR00168##

Synthesis of Compound 34

[0442] Compound 31 (4.85 mg, 0.005 mmol) and gallium trichloride (1.76 mg, 0.010 mmol) were added to water (0.2 mL), and the reaction solution was heated and stirred at 90 C. for 5 minutes. The reaction solution was cooled to room temperature, and the reaction solution was directly separated by Pre-HPLC to obtain 34 (3.5 mg, yield: 67.57%). LC-MS (ESI): m/z=1036.77(M+H).sup.+.

Embodiment 35

##STR00169##

Synthesis of Compound 35

[0443] Compound 9 (5.32 mg, 0.005 mmol) and gallium trichloride (1.76 mg, 0.010 mmol) were added to water (0.2 mL), and the reaction solution was heated and stirred at 90 C. for 10 minutes. The reaction solution was cooled to room temperature, and directly separated by Pre-HPLC to obtain 35 (2.3 mg, yield: 40.71%). LC-MS (ESI): m/z=1131.91(M+H).sup.+.

Embodiment 36

##STR00170##

Synthesis of Compound 36

[0444] Compound 18 (5.18 mg, 0.005 mmol) and gallium trichloride (1.76 mg, 0.010 mmol) were added to water (0.2 mL), and the reaction solution was stirred at 90 C. for 10 minutes. The reaction solution was cooled to room temperature, and directly separated by Pre-HPLC to obtain 36 (2.7 mg, yield: 49.00%). LC-MS (ESI): m/z=1103.86(M+H).sup.+.

Embodiment 37

##STR00171##

Synthesis of Compound 37

[0445] Compound 19 (9.79 mg, 0.01 mmol) and gallium trichloride (3.52, 0.020 mmol) were added to water (0.5 mL), and the reaction solution was heated and stirred at 90 C. for 10 minutes, and the reaction solution was cooled to room temperature. The reaction solution was directly separated by Pre-HPLC to obtain 37 (8.5 mg, yield: 81.26%). LC-MS (ESI): m/z=1146.81(M+H).sup.+.

Embodiment 38

##STR00172##

Synthesis of Compound 38

[0446] Compound 18 (15.54 mg, 0.015 mmol) and lutetium trichloride (8.44 mg, 0.030 mmol) were added to sodium acetate-acetic acid buffer (pH=4.5) (1.0 mL), and the reaction solution was stirred at room temperature for 10 minutes, and directly separated by Pre-HPLC to obtain 38 (8 mg, yield: 44.15%). LC-MS (ESI): m/z=1209.1(M+H).sup.+.

Embodiment 39

##STR00173## ##STR00174##

Synthesis of Compound 39

[0447] Compound 2-c (441.32 mg, 0.80 mmol) and 1,8-dibromo-3,6-dioxoctane (242.85 mg, 0.880 mmol) were dissolved in N, N-dimethylformamide (3.0 mL), and potassium carbonate (143.73 mg, 1.040 mmol) was added. The reaction solution was stirred at 80 C. for 60 hours. The reaction solution was cooled to room temperature, diluted with ethyl acetate (40 mL), and the reaction solution was washed sequentially with water (20 mL2) and saturated brine (20 mL1). The organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was separated by silica gel column chromatography (petroleum ether:ethyl acetate=3:1) to obtain 39-b (240 mg, yield: 40.18%).

Synthesis of Compound 39-a

[0448] Compound 39-b (140 mg, 0.187 mmol) and 2-methylpropan-2-yl (4,7-bis{2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl}-1,4,7,10-tetraazacyclododecan-1-yl) acetate (96.50 mg, 0.187 mmol) were dissolved in acetonitrile (2 mL), and potassium carbonate (25.91 mg, 0.187 mmol) was added, and the reaction solution was stirred at 60 C. for 16 hours. The reaction solution was cooled to room temperature, and the reaction solution was concentrated under reduced pressure, and the residue was purified by Pre-HPLC to obtain 39-a (240 mg, yield: 84.29%).

Synthesis of Compound 39

[0449] Compound 39-a (240 mg, 0.158 mmol) and trifluoroacetic acid (3.0 mL) were dissolved in dichloromethane (3.0 mL), and the reaction solution was stirred at room temperature for 16 hours. The reaction solution was concentrated under reduced pressure. The residue was purified by Pre-HPLC to obtain 39 (78 mg, yield: 51.76%). LC-MS (ESI): m/z=956.24(M+H).sup.+.

Embodiment 40

##STR00175## ##STR00176##

Synthesis of Compound 40-f

[0450] 3-Bromo-1-chloro-2-toluene (3082.20 mg, 15.00 mmol), 4,4,5,5-tetramethyl-2-vinyl-1,3,2-dioxyborane (2772.36 mg, 18.000 mmol), and triethylamine (20.850 mL, 150.000 mmol) were dissolved in toluene (30 mL), and bis(tri-tert-butylphosphine) palladium (383.29 mg, 0.750 mmol) was added, and the reaction solution was replaced with nitrogen for three times, and the reaction solution was heated at 80 C. for 16 hours. The reaction solution was cooled to room temperature, filtered, and the filtrate was concentrated under reduced pressure, and the residue was separated by silica gel column chromatography (petroleum ether:ethyl acetate=10:1) to obtain 40-f (1000 mg, yield: 23.93%).

Synthesis of Compound 40-e

[0451] Compound 2-d (1200 mg, 2.738 mmol) and compound 40-f (991.60 mg, 3.559 mmol) were dissolved in dioxane (10.0 mL) and water (2.0 mL), and (1,1-bis(diphenylphosphino)ferrocene) dichloropalladium (100.17 mg, 0.137 mmol) and potassium carbonate (756.83 mg, 5.476 mmol) were added, and the reaction solution was heated and stirred at 80 C. for 16 hours under nitrogen protection. The reaction solution was cooled to room temperature, and the reaction solution was diluted with water (10 mL), and the mixture was extracted with dichloromethane (30 mL2). The organic phases were combined, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was separated by column chromatography (petroleum ether:ethyl acetate=20:1) to obtain 40-e (220 mg, yield: 15.76%). LC-MS (ESI): m/z=510.39 (M+H).sup.+.

Synthesis of Compound 40-d

[0452] Compound 40-e (220 mg, 0.431 mmol) and 4,4,5,5-tetramethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3,2-dioxaborolane (219.09 mg, 0.863 mmol) were dissolved in toluene (3 mL), and palladium acetate (9.68 mg, 0.043 mmol), 2-dicyclohexylphosphino-2,4,6-triisopropylbiphenyl (41.13 mg, 0.086 mmol), and potassium acetate (84.60 mg, 0.862 mmol) were added, and the reaction solution was heated at 100 C. for 16 hours under nitrogen protection. The reaction solution was cooled to room temperature, and the reaction solution was diluted with dichloromethane (40 mL), and the mixture was washed with water (10 mL1). The organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was separated by column chromatography (petroleum ether:ethyl acetate=10:1) to obtain 40-d (220 mg, yield: 84.86%).

Synthesis of Compound 40-c

[0453] Compound 40-d (220 mg, 0.366 mmol) and 4-{3-[(3-bromo-2-methylphenyl)oxy]propyl}-1,4-oxazinane (137.91 mg, 0.439 mmol) were dissolved in dioxane (2.0 mL) and water (0.4 mL), and (1,1-bis(diphenylphosphino)ferrocene) dichloropalladium (26.76 mg, 0.037 mmol) and potassium carbonate (101.10 mg, 0.731 mmol) were added, and the reaction solution was heated and stirred at 90 C. for 16 hours under nitrogen protection. The reaction solution was cooled to room temperature, and the reaction solution was diluted with water (10 mL), and the obtained mixture was extracted with dichloromethane (40 mL). The organic phase was dried over anhydrous sodium sulfate, concentrated under reduced pressure, and the residue was separated by column chromatography (100% ethyl acetate) to obtain 40-c (195 mg, yield: 75.21%).

Synthesis of Compound 40-b

[0454] Compound 40-c (195 mg, 0.275 mmol) and 1-bromo-2-[(2-bromoethyl)oxy]ethane (191.39 mg, 0.825 mmol) were dissolved in N, N-dimethylformamide (2.0 mL), and potassium carbonate (76.02 mg, 0.550 mmol) was added, and the reaction solution was heated and stirred at 70 C. for 20 hours. The reaction solution was cooled to room temperature and concentrated under reduced pressure, and the residue was separated by column chromatography (ethyl acetate:ethanol=20:1) to obtain 40-b (150 mg, yield: 63.44%).

Synthesis of Compound 40-a

[0455] Compound 40-b (150 mg, 0.174 mmol) and 2-methylpropan-2-yl (4,7-bis{2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl}-1,4,7,10-tetraazacyclododecan-1-yl) acetate (134.68 mg, 0.262 mmol) were dissolved in acetonitrile (2.0 mL), and potassium carbonate (36.17 mg, 0.262 mmol) was added, and the reaction solution was stirred at 60 C. for 16 hours, and 13% of 40-b was remained and the mixture was continuously heated and stirred for 8 hours. The reaction solution was evaporated to dryness, and the residue was separated by column chromatography (methanol:ammonia methanol (7 M)=5:1) to obtain 40-a (170 mg, yield: 75.33%).

Synthesis of Compound 40

[0456] Compound 40-a (170 mg, 0.131 mmol) was dissolved in dichloromethane (5.0 mL), and trifluoroacetic acid (5.0 mL) was added. The reaction solution was stirred at room temperature for 16 hours. The reaction solution was concentrated under reduced pressure, and the residue was separated by Pre-HPLC to obtain 40 (40 mg, yield: 21.64%).

Embodiment 41

##STR00177##

Synthesis of Compound 41

[0457] Compound 39 (11.2 mg, 0.012 mmol) and lutetium trichloride (7.25 mg, 0.026 mmol) were dissolved in sodium acetate-acetic acid buffer (pH=4.5) (0.5 mL), and the reaction solution was heated at 90 C. for 20 minutes. The reaction solution was cooled to room temperature, and purified directly by Pre-HPLC to obtain 41 (11 mg, yield: 83.27%).

Embodiment 42

##STR00178##

Synthesis of Compound 42-e

[0458] 2-Chloro-4-phenylpyridine-3-carbonitrile (4293.20 mg, 20.00 mmol) and 4,4,5,5-tetramethyl-2-vinyl-1,3,2-dioxyborane (7701.00 mg, 50.00 mmol) were dissolved in dioxane (50.0 mL) and water (10.0 mL), and potassium carbonate (8292.60 mg, 60.00 mmol) and (1,1-bis(diphenylphosphino)ferrocene) dichloropalladium (1463.40 mg, 2.00 mmol) were mixed in a microwave tube, and the microwave tube was sealed after 1 minute of nitrogen substitution. The reaction solution was stirred at 100 C. for 16 hours, and the reaction solution was cooled to room temperature. The reaction solution was directly diluted with water (50 mL), and extracted with dichloromethane (100 mL). The organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was separated by column chromatography (petroleum ether:ethyl acetate=85:15) to obtain 42-e (3150 mg, yield: 76.36%). LC-MS (ESI): m/z=207.29(M+H).sup.+.

Synthesis of Compound 42-d

[0459] Compound 42-e (412.50 mg, 2.0 mmol) and compound 2-d (876.56 mg, 2.00 mmol) were dissolved in N, N-dimethylacetamide (6.0 mL), and palladium acetate (44.90 mg, 0.20 mmol), tri(o-tolyl)phosphine (121.75 mg, 0.40 mmol), and triethylamine (2.0 mL, 14.389 mmol) were added, and the mixture was heated via microwave at 160 C. for 0.5 hour under nitrogen protection. The reaction solution was cooled to room temperature and concentrated under reduced pressure, and the residue was separated by column chromatography (petroleum ether:ethyl acetate=5:1) to obtain 42-d (550 mg, yield: 48.79%).

Synthesis of Compound 42-c

[0460] Compound 42-d (225.45 mg, 0.4 mmol) and 2-methylpropan-2-yl-4-(iodomethyl) hexahydropyridine-1-carboxylate (650.38 mg, 2.00 mmol) were dissolved in N, N-dimethylformamide (2 mL), and potassium carbonate (276.42 mg, 2.00 mmol) was added, and the reaction solution was heated and stirred at 80 C. for 60 hours. The reaction solution was cooled to room temperature, diluted with ethyl acetate (40 mL), and washed sequentially with water (20 mL2) and saturated brine (20 mL). The organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was separated by silica gel column chromatography (petroleum ether:ethyl acetate=5:1) to obtain 42-c (248 mg, yield: 81.48%).

Synthesis of Compound 42-b

[0461] Compound 42-c (248 mg, 0.326 mmol) was dissolved in tetrahydrofuran (3 mL), and dioxane solution of hydrochloric acid (1 mL) was added. The reaction solution was stirred at room temperature for 6 hours. 1 M K.sub.2CO.sub.3 solution (10 mL) was added. The mixture was extracted with dichloromethane (30 mL). The separated organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain 42-b (215 mg, yield: 99.83%). The product 42-b was directly used in the next step of reaction without purification.

Synthesis of Compound 42-a

[0462] Compound 42-b (100 mg, 0.151 mmol), (10-{1-[(2-methylpropan-2-yl)oxy]-1-oxoethyl-2-yl}-4,7-bis{2-[(2-methylpropan-2-yl)oxy)-2-oxoethyl}-1,4,7,10-tetraazacyclododecan-1-yl) acetic acid (104.01 mg, 0.182 mmol) and O-benzotriazole-tetramethyluronium hexafluorophosphate (74.61 mg, 0.197 mmol) were dissolved in N, N-dimethylformamide (1.0 mL), and diisopropylethylamine (0.050 mL, 0.303 mmol) was added, and the reaction solution was stirred at room temperature for 1 hour. The reaction solution was concentrated under reduced pressure, and the residue was separated by silica gel column chromatography (petroleum ether:ethyl acetate:ethanol=10:20:1) to obtain 42-a (360 mg, yield: 78.89%).

Synthesis of Compound 42

[0463] Compound 42-a (150 mg, 0.096 mmol) was dissolved in dichloromethane (2.0 mL), and trifluoroacetic acid (2.0 mL) was added. The reaction solution was stirred at room temperature for 20 hours. The reaction solution was concentrated under reduced pressure, and the residue was separated by Pre-HPLC to obtain 42 (63 mg, yield: 66.01%).

Embodiment 43

##STR00179##

Synthesis of Compound 43-c

[0464] Compound 42-d (112.72 mg, 0.2 mmol), 1,4-diiodobutane (247.94 mg, 0.80 mmol) was dissolved in N, N-dimethylformamide (1.0 mL), and potassium carbonate (55.28 mg, 0.40 mmol) was added, and the reaction solution was stirred at 50 C. for 1 hour. The reaction solution was cooled to room temperature, and the reaction solution was diluted with ethyl acetate (50 mL), washed sequentially with water (20 mL2) and saturated brine (20 mL). The organic phase was separated, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was separated by column chromatography (petroleum ether:ethyl acetate=5:1) to obtain 43-c (124 mg, yield: 83.15%).

Synthesis of Compound 43-b

[0465] Compound 43-c (124 mg, 0.166 mmol) was dissolved in tetrahydrofuran (3 mL), and ammonia methanol solution (10 mL, 70.00 mmol) was added. The reaction solution was heated and stirred at 50 C. for 16 hours. The reaction solution was cooled to room temperature and concentrated under reduced pressure, and the residue was dissolved in dichloromethane (30 mL) and washed with 1 M K.sub.2CO.sub.3 solution (10 mL). The separated organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain 43-b (105 mg, yield: 99.47%), which was directly used in the next step of reaction without purification.

Synthesis of Compound 43-a

[0466] Compound 43-b (105 mg, 0.165 mmol), (4,7,10-tris{2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl}-1,4,7,10-tetraazacyclododecan-1-yl)acetic acid (113.69 mg, 0.199 mmol), and O-benzotriazole-tetramethyluronium hexafluorophosphate (81.56 mg, 0.215 mmol) were dissolved in acetonitrile (1.0 mL), and diisopropylethylamine (0.055 mL, 0.331 mmol) was added. The reaction solution was stirred at room temperature for 1 hour. The reaction solution was concentrated under reduced pressure, and the residue was separated by column chromatography (dichloromethane:methanol=94:6) to obtain 43-a (196 mg, yield: 99.61%).

Synthesis of Compound 43

[0467] Compound 43-a (196 mg, 0.165 mmol) was dissolved in dichloromethane (3.0 mL). Trifluoroacetic acid (3.0 mL) was added. The reaction solution was stirred at room temperature for 20 hours. The reaction solution was concentrated under reduced pressure, and the residue was separated by Pre-HPLC to obtain compound 43 (80 mg, yield: 50.31%). LC-MS (ESI): m/z=965.45 (M+H).sup.+.

Embodiment 44

##STR00180##

Synthesis of Compound 44

[0468] Compound 42 (9.91 mg, 0.01 mmol) was dissolved in sodium acetate-acetic acid buffer (pH=4.5) (0.5 mL), and lutetium trichloride (5.63 mg, 0.020 mmol) was added, and the reaction solution was stirred at 90 C. for 10 minutes. The reaction solution was cooled to room temperature, and separated directly by Pre-HPLC to obtain 44 (10.6 mg, yield: 91.14%). LC-MS (ESI): m/z=1163.12 (M+H).sup.+.

Embodiment 45

##STR00181##

Synthesis of Compound 45

[0469] Compound 43 (11 mg, 0.011 mmol) and lutetium trichloride (9.28 mg, 0.033 mmol) were dissolved in sodium acetate-acetic acid buffer (pH=4.5) (0.5 mL), and the reaction solution was stirred at 90 C. for 10 minutes. The reaction solution was directly separated by Pre-HPLC to obtain 45 (9 mg, yield: 71.94%). LC-MS (ESI): m/z=1137.80 (M+H).sup..

Embodiment 46

##STR00182##

Synthesis of Compound 46

[0470] Compound 40 (15 mg, 0.011 mmol) was dissolved in sodium acetate-acetic acid buffer (pH=4.5) (0.5 mL), and lutetium trichloride (5.98 mg, 0.021 mmol) was added. The reaction solution was heated and stirred at 90 C. for 10 minutes. The reaction solution was cooled to room temperature, and purified directly by Pre-HPLC to obtain 46 (5.5 mg, yield: 41.70%).

Embodiment 47

##STR00183##

Synthesis of Compound 47-b

[0471] A solution of 2-methylpropan-2-yl bromoacetate (3019.14 mg, 15.478 mmol) dissolved in acetonitrile (40 mL) was added dropwise into a solution of 1,4,7-triazane (1000 mg, 7.739 mmol) dissolved in acetonitrile (10 mL) at 0 C. After dropwise addition, the reaction solution was stirred at room temperature for 24 hours, and the reaction solution was concentrated under reduced pressure, and diluted with pure water (5 mL). The mixture was adjusted to pH=3 with 1 M hydrochloric acid. The reaction solution was extracted with methyl tert-butyl ether (15 mL3), and the mixture was adjusted to PH=8 with 1 M sodium hydroxide solution, extracted with dichloromethane (20 mL2), and the organic phases were combined, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain 47-b (1200 mg, yield: 43.37%).

Synthesis of Compound 47-a

[0472] Compound 2-b (140.53 mg, 0.20 mmol) and compound 47-b were dissolved in acetonitrile (1.0 mL), and potassium carbonate (55.28 mg, 0.400 mmol) was added, and the reaction solution was stirred at 60 C. overnight. The reaction solution was cooled to room temperature, concentrated under reduced pressure, and the residue was separated by column chromatography (dichloromethane:methanol=5:1) to obtain 47-a (153 mg, yield: 78.12%).

Synthesis of Compound 47

[0473] Compound 47-a (153 mg, 0.156 mmol) was dissolved in dichloromethane (2.5 mL), and trifluoroacetic acid (2.5 mL) was added. The reaction solution was stirred at room temperature overnight. The reaction solution was concentrated under reduced pressure, and the residue was separated by Pre-HPLC to obtain 47 (75 mg, yield: 59.19%).

Embodiment 48

##STR00184##

Synthesis of Compound 48

[0474] Aluminum chloride (0.80 mg, 0.006 mmol) was dissolved in 0.2 M sodium acetate-acetic acid buffer (pH=4.5) (0.60 mL), and sodium fluoride (0.25 mg, 0.006 mmol) was added, and the reaction solution was stirred at room temperature for 5 minutes. Compound 47 (4.05 mg, 0.005 mmol) was added, and the mixture was heated at 100 C. for 15 minutes. The reaction solution was cooled to room temperature, and the reaction solution was purified directly by Pre-HPLC to obtain 48 (3.0 mg, yield: 70.26%).

Embodiment 49

##STR00185##

Synthesis of Compound 49-d

[0475] 4,4,5,5-Tetramethyl-2-[(1E)-2-(2-methyl-3-phenylphenyl)vinyl]-1,3,2-dioxyborane (960.7 mg, 3.0 mmol) and 4-bromo-2-hydroxy-5-methylphenyl-1-formaldehyde (645.1 mg, 3.00 mmol) were dissolved in dioxane (100.0 mL) and water (20.0 mL), and (1,1-bis(diphenylphosphino)ferrocene)dichloropalladium (219.3 mg, 0.3 mmol) and potassium carbonate (1243.8 mg, 9.00 mmol) were added. The reaction solution was heated and stirred at 90 C. for 12 hours, and the reaction solution was cooled to room temperature, concentrated under reduced pressure, and the residue was purified by column chromatography (petroleum ether:ethyl acetate=10:1) to obtain 49-d (950 mg, yield: 86.78). LC-MS (ESI): m/z=329.1(M+Na)*.

Synthesis of Compound 49-c

[0476] Compound 49-d (620 mg, 2.89 mmol) and 1-bromo-2-[(2-bromoethyl)oxy]ethane (875.6 mg, 3.77 mmol) were dissolved in N, N-dimethylformamide (50 m1), and potassium carbonate (782.7 mg, 5.66 mmol) was added, and the reaction solution was stirred at 70 C. for 12 hours. The reaction solution was cooled to room temperature, concentrated under reduced pressure, and the residue was dissolved with dichloromethane (100 mL), and the mixture was washed sequentially with water (50 ml2) and saturated brine (50 m1), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was purified by column chromatography (petroleum ether:ethyl acetate=3:1) to obtain 49-c (220 mg, yield: 23.09%).

Synthesis of Compound 49-b

[0477] Compound 49-c (280.0 mg, 0.58 mmol) and compound 2-e (216.41 mg, 1.16 mmol) were dissolved in methanol (40 mL), and sodium cyanoborohydride (110.39 mg, 1.752 mmol) and acetic acid (35.0 mg, 0.584 mmol) were added, and the reaction solution was stirred at 60 C. for 6 hours. The reaction solution was cooled to room temperature and concentrated under reduced pressure, and the concentrate was separated by column chromatography (petroleum ether:ethyl acetate=10:1) to obtain 49-b (280 mg, yield: 70.21%). LC-MS (ESI): m/z=648.3 (M+H).sup.+.

Synthesis of Compound 49-a

[0478] Compound 49-b (380 mg, 0.586 mmol) and compound 47-b (418.8 mg, 1.172 mmol) were dissolved in acetonitrile (30.0 mL), and potassium carbonate (323.36 mg, 2.343 mmol) was added. The reaction solution was stirred at 60 C. for 12 hours, and the reaction solution was cooled to room temperature and concentrated under reduced pressure, and the residue was dissolved in dichloromethane (100 mL). The mixture was washed sequentially with water (50 ml2) and saturated brine (50 m1), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was purified by column chromatography (petroleum ether:ethyl acetate=10:1) to obtain 49-a (320 mg, yield: 56.09%).

Synthesis of Compound 49

[0479] Compound 49-a (320 mg, 0.346 mmol) was dissolved in dichloromethane (20.0 mL) and trifluoroacetic acid (20 mL) was added. The reaction solution was stirred at room temperature for 12 hours and concentrated under reduced pressure, and the residue was directly separated by pre-HPLC to obtain 49 (52 mg, yield: 19.86%). LC-MS (ESI): m/z=757.5(M+H).sup.+.

Embodiment 50

##STR00186##

Synthesis of Compound 50

1. Preparation of [AlF].SUP.2+ Solution

[0480] AlCl.sub.3 (100 mg) was dissolved in 0.2 M AcONa/AcoH buffer (50 mL), and the solution was shaken well and set aside. NaF (50 mg) and 0.2 M AcONa/AcoH buffer (40 mL) were added to a plastic (centrifuge) tube with cover, and the solution was shaken well and set aside. The above AlCl.sub.3 solution (10.0 mL) was added to the plastic (centrifuge) tube, then NaF solution (5.0 mL) was added. The mixture was shaken for 2 minutes, and set aside.

[0481] 2. Compound 49 (1.0 mg, 0.13 mmol) was dissolved in anhydrous ethanol (0.6 mL), and [AlF].sup.2+ solution (0.016 mmol, 1.6 mL) prepared above was added, and the reaction solution was stirred at 100 C. for 30 minutes. The reaction solution was cooled to room temperature and concentrated under reduced pressure, and the residue was directly separated by prep-HPLC to obtain 50 (6.2 mg, yield: 58.6%). LC-MS (ESI): m/z=801.2(M+H).sup.+.

Embodiment 51

##STR00187##

Synthesis of Compound 51-d

[0482] The compound butane-1,4-diol (901.2 mg, 10.0 mmol) was dissolved in dichloromethane (50.0 mL), and pyridine (3160.0 mg, 40.0 mmol) was added, and the reaction solution was cooled to 0 C., then 4-methylbenzenesulfonyl chloride (5719.5 mg, 30.00 mmol) was added. The reaction solution was stirred at room temperature overnight, concentrated under reduced pressure, and the residue was dissolved with ethyl acetate (100 mL), and the mixture was washed with water (50.0 mL2), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was purified by column chromatography (petroleum ether:ethyl acetate=15:1) to obtain 51-d (670 mg, yield: 16.8%). LC-MS (ESI): m/z=329.1(M+Na)*.

Synthesis of Compound 51-c

[0483] Compound 49-d (656.8 mg, 2.0 mmol) and compound 51-d (1594.0 mg, 4.0 mmol) were dissolved in N, N-dimethylformamide (50.0 mL), and potassium carbonate (1382.0 mg, 10.0 mmol) was added. The reaction solution was heated and stirred at 50 C. for 6 hours, and the reaction solution was cooled to room temperature. The reaction solution was concentrated under reduced pressure, and the residue was dissolved in dichloromethane (100 mL), and the mixture was washed sequentially with water (50 ml2) and saturated brine (50 m1), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was purified by column chromatography (petroleum ether:ethyl acetate=3:1) to obtain 51-c (610 mg, yield: 54.98%). LC-MS (ESI): m/z=555.2(M+H).sup.+.

Synthesis of Compound 51-b

[0484] Compound 51-c (554.7 mg, 1.0 mmol) and compound 2-e (555.8 mg, 3.0 mmol) were dissolved in methanol (40 mL), and sodium cyanoborohydride (126.0 mg, 2.0 mmol) and acetic acid (120.0 mg, 2.0 mmol) were added. The reaction solution was stirred at 60 C. for 6 hours. The reaction solution was cooled to room temperature and concentrated under reduced pressure, and the residue was separated by column chromatography (petroleum ether:ethyl acetate=10:1) to obtain 51-b (370 mg, yield: 51.1%). LC-MS (ESI): m/z=724.6(M+H).sup.+.

Synthesis of Compound 51-a

[0485] Compound 57-b (370 mg, 0.511 mmol) and compound 47-b (365.4 mg, 1.02 mmol) were dissolved in acetonitrile (30.0 mL), and potassium carbonate (282.1 mg, 2.04 mmol) was added. The reaction solution was heated and stirred at 60 C. for 12 hours, and the reaction solution was cooled to room temperature and concentrated under reduced pressure. The residue was dissolved in dichloromethane (100 mL), and the mixture was washed sequentially with water (50 ml2) and saturated brine (50 m1), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was purified by column chromatography (dichloromethane:methanol=10:1) to obtain 51-a (350 mg, yield: 75.32%). LC-MS (ESI): m/z=926.2(M+H).sup.+.

Synthesis of Compound 51

[0486] Compound 51-a (350 mg, 0.385 mmol) was dissolved in dichloromethane (20.0 mL), and trifluoroacetic acid (20 mL) was added, and the reaction solution was stirred at room temperature for 12 hours and concentrated under reduced pressure, and the residue was directly separated by pre-HPLC to obtain 51 (158 mg, yield: 55.4%). LC-MS (ESI): m/z=741.5(M+H).sup.+.

Embodiment 52

##STR00188##

Synthesis of Compound 52

[0487] Compound 51 (20 mmol, 0.027 mg) was dissolved in anhydrous ethanol (0.5 mL), and the [AlF].sup.2+ solution (0.016 mmol, 1.6 mL) prepared in Embodiment 50 was added, and the reaction solution was stirred at 100 C. for 30 minutes. The reaction solution was cooled to room temperature, and directly separated by prep-HPLC to obtain 52 (15 mg, yield: 70.79%). LC-MS (ESI): m/z=785.2(M+H).sup.+.

Embodiment 53

##STR00189##

Synthesis of Compound 53-c

[0488] Compound 49-d (328.4 mg, 1.0 mmol) and 1,5-diiodopentane (647.8 mg, 2.0 mmol) were dissolved in N, N-dimethylformamide (20.0 mL), and potassium carbonate (414.6 mg, 3.0 mmol) was added. The reaction solution was stirred at room temperature for 12 hours, and water (60 mL) was added, and the mixture was extracted with dichloromethane (150 mL). The organic phases were combined, washed sequentially with water (50 m12) and saturated brine (50 m1), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was purified by column chromatography (petroleum ether:ethyl acetate=10:1) to obtain 53-c (55 mg, yield: 9.96%). LC-MS (ESI): m/z=525.2 (M+H).sup.+.

Synthesis of Compound 53-b

[0489] Compound 53-c (340 mg, 0.648 mmol) and compound 2-e (240.23 mg, 1.297 mmol) were dissolved in methanol (40 mL), and sodium cyanoborohydride (81.69 mg, 1.29 mmol) and acetic acid (77.8 mg, 1.29 mmol) were added. The reaction solution was heated and stirred at 60 C. for 5 hours, and the reaction solution was cooled to room temperature and concentrated under reduced pressure, and the residue was separated by column chromatography (petroleum ether:ethyl acetate=10:1) to obtain 53-b (158 mg, yield: 55.4%). LC-MS (ESI): m/z=694.8 (M+H).sup.+.

Synthesis of Compound 53-a

[0490] Compound 53-b (230 mg, 0.332 mmol) and compound 47-b (237.0 mg, 0.663 mmol) were dissolved in acetonitrile (30.0 mL), and potassium carbonate (137.2 mg, 0.995 mol) was added. The reaction solution was heated and stirred at 65 C. for 12 hours, and the reaction solution was cooled to room temperature, concentrated under reduced pressure, and the residue was dissolved in dichloromethane (100 mL). The mixture was washed sequentially with water (50 ml2) and saturated brine (50 m1), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was purified by column chromatography (petroleum ether:ethyl acetate=10:1) to obtain 53-a (230 mg, yield: 75.13%). LC-MS (ESI): m/z=923.7 (M+H).sup.+.

Synthesis of Compound 53

[0491] Compound 53-a (230 mg, 0.249 mmol) was dissolved in dichloromethane (20.0 mL), and trifluoroacetic acid (10.0 mL) was added. The reaction solution was stirred at room temperature for 18 hours, and the reaction solution was concentrated under reduced pressure, and the residue was directly separated by pre-HPLC to obtain 53 (110.3 mg, yield: 58.65%). LC-MS (ESI): m/z=755.7 (M+H).sup.+.

Embodiment 54

##STR00190##

Synthesis of Compound 54

[0492] Compound 53 (0.033 mmol, 25.0 mg) was dissolved in anhydrous ethanol (0.5 mL), and the [AlF].sup.2+ solution (0.016 mmol, 1.6 mL) prepared in Embodiment 50 was added, and the reaction solution was heated and stirred at 100 C. for 30 minutes. The reaction solution was cooled to room temperature, and directly separated by prep-HPLC to obtain 54 (14.1 mg, yield: 53.29%). LC-MS (ESI): m/z=800.6 (M+H).sup.+.

Embodiment 55

##STR00191##

Synthesis of Compound 55-c

[0493] Compound 49-d (328.41 mg, 1.0 mmol) and 1,6-diiodohexane (675.94 mg, 2.0 mmol) were dissolved in N, N-dimethylformamide (30.0 mL), and potassium carbonate (414.60 mg, 3.0 mmol) was added. The reaction solution was stirred at room temperature for 12 hours and concentrated under reduced pressure, and the residue was dissolved in dichloromethane (100 mL). The mixture was washed sequentially with water (50 m12) and saturated brine (50 m1), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was purified by column chromatography (petroleum ether:ethyl acetate=10:1) to obtain 55-c (380 mg, yield: 67.04%). LC-MS (ESI): m/z=539.2 (M+H).sup.+.

Synthesis of Compound 55-b

[0494] Compound 55-c (340 mg, 0.631 mmol) and compound 2-e (240.0 mg, 1.263 mmol) were dissolved in methanol (40 mL), and sodium cyanoborohydride (79.56 mg, 1.26 mmol) and acetic acid (75.8 mg, 1.26 mmol) were added. The reaction solution was heated and stirred at 60 C. for 5 hours, and the reaction solution was cooled to room temperature and concentrated under reduced pressure, and the residue was purified by column chromatography (petroleum ether:ethyl acetate=10:1) to obtain 55-b (230 mg, yield: 51.47%). LC-MS (ESI): m/z=709.8 (M+H).sup.+.

Synthesis of Compound 55-a

[0495] Compound 55-b (380 mg, 0.586 mmol) and compound 47-b (418.8 mg, 1.172 mmol) were dissolved in acetonitrile (30.0 mL), and potassium carbonate (323.36 mg, 2.343 mmol) was added, and the reaction solution was heated and stirred at 60 C. for 12 hours. The reaction solution was cooled to room temperature and concentrated under reduced pressure, and the residue was dissolved in dichloromethane (100 mL). The mixture was washed sequentially with water (50 ml2) and saturated brine (50 mlxi), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was purified by column chromatography (petroleum ether:ethyl acetate=10:1) to obtain 55-a (180 mg, yield: 61.78%). LC-MS (ESI): m/z=926.2 (M+H).sup.+.

Synthesis of Compound 55

[0496] Compound 55-a (220 mg, 0.235 mmol) was dissolved in dichloromethane (20.0 mL), and trifluoroacetic acid (10.0 mL) was added, and the reaction solution was stirred at room temperature for 12 hours and concentrated under reduced pressure, and the residue was directly separated by pre-HPLC to obtain 55 (160 mg, yield: 88.65%). LC-MS (ESI): m/z=769.6 (M+H).sup.+.

Embodiment 56

##STR00192##

Synthesis of Compound 56

[0497] Compound 55 (0.039 mmol, 6.0 mg) was dissolved in anhydrous ethanol (1.0 mL), and the [AlF].sup.2+ solution (0.05 mmol, 5.0 mL) prepared in Embodiment 50 was added, and the reaction solution was heated and stirred at 100 C. for 30 minutes. The reaction solution was cooled to room temperature, and directly separated by prep-HPLC to obtain 56 (6 mg, yield: 18.92%). LC-MS (ESI): m/z=814.6 (M+H).sup.+.

Embodiment 57

##STR00193## ##STR00194##

Synthesis of Compound 57-b

[0498] Compound 42-d (195 mg, 0.346 mmol) and 1,5-diiodopentane (224.15 mg, 0.692 mmol) were dissolved in N, N-dimethylformamide (5 mL), and potassium carbonate (239.09 mg, 1.730 mmol) was added, and the reaction solution was stirred at 60 C. for 1 hour. The reaction solution was cooled to room temperature, and the reaction solution was extracted with ethyl acetate (10 mL), washed sequentially with water (10 mL3) and saturated brine (10 mL1), and the organic phases were combined, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain 57-b (211 mg, yield: 80.49%).

Synthesis of Compound 57-a

[0499] Compound 57-b (211 mg, 0.278 mmol) and compound 47-b were dissolved in acetonitrile (10 mL), and potassium carbonate (76.98 mg, 0.557 mmol) was added, and the reaction solution was stirred at 60 C. overnight. The reaction solution was cooled to room temperature and concentrated under reduced pressure, and the residue was dissolved with ethyl acetate (10 mL), and the mixture was washed sequentially with water (10 mL3) and saturated brine (10 mL1). The organic phases were combined, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain 57-a (242 mg, yield: 87.85%).

Synthesis of Compound 57

[0500] Compound 57-a (242 mg, 0.245 mmol) was dissolved in dichloromethane (9 mL), and trifluoroacetic acid (9 mL, 1.223 mmol) was added. The reaction solution was stirred at room temperature for 30 minutes, and the reaction solution was concentrated under reduced pressure, and the residue was separated by prep-HPLC to obtain 57 (93.61 mg, yield: 46.61%).

Embodiment 58

##STR00195##

Synthesis of Compound 58

[0501] Compound 57 (20 mg, 0.024 mmol) was dissolved in ethanol (0.50 mL), and 0.2 M sodium acetate-acetic acid buffer (pH=4.6) (1.0 mL), aluminum chloride (2 mg, 0.029 mmol), and sodium fluoride (1 mg, 0.029 mmol) were added, and the reaction solution was stirred at 100 C. for 30 minutes. The reaction solution was cooled to room temperature and concentrated under reduced pressure, and the residue was separated by prep-HPLC to obtain 58 (11.68 mg, yield: 55.43%).

Embodiment 59

##STR00196##

Synthesis of Compound 59-b

[0502] Compound 47-b (715.00 mg, 2.0 mmol) and potassium carbonate (552.84 mg, 4.00 mmol) were dissolved in methanol (10 mL) and water (10 mL), and bromoacetic acid (383.48 mg, 2.76 mmol) was added. The reaction solution was stirred at room temperature overnight, and the pH was adjusted to 6 with hydrochloric acid (1 mol/L), and the reaction solution was extracted with dichloromethane (50 mL2). The organic phases were combined, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain 59-b (610 mg, yield: 73.40%).

Synthesis of Compound 59-a

[0503] Compound 42-b (115 mg, 0.174 mmol) was dissolved in N, N-dimethylformamide (5 mL), and 59-b (86.78 mg, 0.209 mmol), O-benzotriazole-tetramethyluronium hexafluorophosphate (85.80 mg, 0.226 mmol), and diisopropylethylamine (0.058 mL, 0.348 mmol) were added, and the reaction solution was stirred at room temperature for 1 hour. The reaction solution was extracted with ethyl acetate (10 mL), washed sequentially with water (10 mL3) and saturated brine (10 mL1), and the organic phases were combined, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain 59-a (45.66 mg, yield: 24.79%).

Synthesis of Compound 59

[0504] Compound 59-a (45.66 mg, 0.043 mmol) was dissolved in dichloromethane (9 mL), and trifluoroacetic acid (9 mL, 1.223 mmol) was added, and the reaction solution was stirred at room temperature for 30 minutes. The reaction solution was concentrated under reduced pressure, and directly separated by pre-HPLC to obtain 59 (22.57 mg, yield: 58.78%). LC-MS (ESI): m/z=890 (M+H).sup.+.

Embodiment 60

##STR00197##

Synthesis of Compound 60

[0505] Compound 59 (5 mg, 0.006 mmol) was dissolved in 0.2 M sodium acetate-acetic acid buffer (pH=4.6) (1.0 mL), and aluminum chloride (AlCl.sub.3, 0.6 mL, 0.002 mmol) and sodium fluoride (0.3 mL, 0.002 mmol) were added, and the reaction solution was stirred at 100 C. for 30 minutes. The reaction solution was cooled to room temperature, and separated directly by prer-HPLC to obtain 60 (1.96 mg, yield: 37.33%). LC-MS (ESI): m/z=934 (M+H).sup.+.

Embodiment 61

##STR00198##

Synthesis of Compound 61-a

[0506] Compound 4-b (124.5 mg, 0.20 mmol) and compound 59-b (108.0 mg, 0.26 mmol) were dissolved in N, N-dimethylformamide (15.0 mL), and O-benzotriazole-tetramethyluronium hexafluorophosphate (113.7 mg, 0.30 mmol) and diisopropylethylamine (77.4 mg, 0.60 mmol) were added, and the reaction solution was stirred at room temperature for 18 hours, diluted with dichloromethane (100 mL), washed sequentially with water (50 ml3) and saturated brine (50 ml1), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was purified by column chromatography (dichloromethane:methanol=10:1) to obtain 61-a (60 mg, yield: 29.81%). LC-MS (ESI): m/z=1020.7 (M+H).sup.+.

Synthesis of Compound 61

[0507] Compound 61-a (60 mg, 0.059 mmol) was dissolved in dichloromethane (12.0 mL), and trifluoroacetic acid (6.0 mL) was added, and the reaction solution was stirred at room temperature for 6 hours and concentrated under reduced pressure, and the residue was directly separated by pre-HPLC to obtain 61 (15 mg, yield: 29.94%). LC-MS (ESI): m/z=852.8 (M+H).sup.+.

Embodiment 62

##STR00199##

Synthesis of Compound 62

[0508] Compound 61 (0.008 mmol, 7.0 mg) was dissolved in anhydrous ethanol (1.0 mL), and the [AlF].sup.2+ solution (0.016 mmol, 1.6 mL) prepared in Embodiment 50 was added, and the reaction solution was heated and stirred at 100 C. for 2 hours. The reaction solution was cooled to room temperature, and directly separated by prep-HPLC to obtain 62 (1.6 mg, yield: 21.74%). LC-MS (ESI): m/z=897.4 (M+H).sup.+.

Embodiment 63

##STR00200## ##STR00201##

Synthesis of Compound 63-c

[0509] Compound 2-c (551.65 mg, 1.0 mmol) and 1,3-dibromopropane (0.305 mL, 3.00 mmol) were dissolved in DMF (5.0 mL), and potassium carbonate (276.42 mg, 2.00 mmol) was added, and the reaction solution was heated and stirred at 50 C. for 7 hours. The reaction solution was cooled to room temperature, diluted with ethyl acetate (50 mL), and washed sequentially with water (20 mL2) and saturated brine (20 mL1). The organic phases were combined, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was separated by column chromatography (petroleum ether:ethyl acetate=20:1) to obtain 63-c (461 mg, yield: 68.54%).

Synthesis of Compound 63-b

[0510] Compound 63-c (461 mg, 0.807 mmol) and ammonia methanol solution (7 M) (23 mL) were sealed in a microwave tube, and the reaction solution was heated and stirred at 50 C. for 60 hours. The reaction solution was cooled to room temperature and concentrated under reduced pressure, and the residue was dissolved in dichloromethane (50 mL) and washed with 10% K.sub.2CO.sub.3 solution (10 mL). The organic phase was separated, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain 63-b (409 mg, yield: 99.89%), which was directly used in the next step of reaction without purification.

Synthesis of Compound 63-a

[0511] Compound 63-b (121.7 mg, 0.20 mmol) and compound 59-b (108.0 mg, 0.26 mmol) were dissolved in N, N-dimethylformamide (15.0 mL), and O-benzotriazole-tetramethyluronium hexafluorophosphate (113.7 mg, 0.30 mmol) and diisopropylethylamine (77.4 mg, 0.60 mmol) were added, and the reaction solution was stirred at room temperature for 18 hours, diluted with dichloromethane (100 mL), washed sequentially with water (50 ml3) and saturated brine (50 ml1), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was separated by column chromatography (dichloromethane:methanol=10:1) to obtain 63-a (90 mg, yield: 44.72%). LC-MS (ESI): m/z=1006.7 (M+H).sup.+.

Synthesis of Compound 63

[0512] Compound 63-a (90 mg, 0.089 mmol) was dissolved in dichloromethane (20.0 mL), and trifluoroacetic acid (10.0 mL) was added, and the reaction solution was stirred at room temperature for 12 hours and concentrated under reduced pressure, and the residue was directly separated by pre-HPLC to obtain 63 (25 mg, yield: 33.36%). LC-MS (ESI): m/z=838.4 (M+H).sup.+.

Embodiment 64

##STR00202##

Synthesis of Compound 64

[0513] Compound 63 (0.008 mmol, 7.0 mg) was dissolved in anhydrous ethanol (1.0 mL), and the [AlF].sup.2+ solution (0.016 mmol, 1.6 mL) prepared in Embodiment 50 was added, and the reaction solution was heated and stirred at 100 C. for 2 hours. The reaction solution was cooled to room temperature, and directly separated by prep-HPLC to obtain 64 (6.67 mg, yield: 70.42%). LC-MS (ESI): m/z=883.4 (M+H).sup.+.

Embodiment 65

##STR00203##

Synthesis of Compound 65-a

[0514] Compound 16-c (252 mg, 0.337 mmol) and compound 47-b (156.64 mg, 0.438 mmol) were dissolved in acetonitrile (3.0 mL), and potassium carbonate (72 mg, 0.521 mmol) was added, and the reaction solution was stirred at room temperature overnight. The reaction solution was concentrated under reduced pressure, and the residue was separated by silica gel column chromatography (dichloromethane:methanol=10:1) to obtain 65-a (190 mg, yield: 57.68%).

Synthesis of Compound 65

[0515] Compound 65-a (190 mg, 0.194 mmol) was dissolved in dichloromethane (3.0 mL), and trifluoroacetic acid (3.0 mL) was added. The reaction solution was stirred at room temperature overnight, and the reaction solution was concentrated under reduced pressure, and directly separated by pre-HPLC to obtain 65 (74 mg, yield: 47.05%). LC-MS (ESI): m/z=809.5(M+H).sup.+.

[0516] .sup.1H NMR (400 MHz, MeOD) 7.90 (s, 1H), 7.62 (d, J=15.9 Hz, 1H), 7.57-7.49 (m, 2H), 7.46-7.38 (m, 2H), 7.38-7.23 (m, 5H), 7.18 (d, J=7.5 Hz, 1H), 4.59 (d, J=13.0 Hz, 1H), 4.42 (d, J=13.0 Hz, 1H), 4.32 (t, J=6.3 Hz, 2H), 3.59 (dd, J=9.9, 3.6 Hz, 1H), 3.56-3.35 (m, 5H), 3.24-2.78 (m, 15H), 2.30 (s, 3H), 2.28-2.16 (m, 1H), 2.06-1.67 (m, 8H), 1.67-1.51 (m, 3H).

Embodiment 66

##STR00204##

Synthesis of Compound 66

[0517] Aluminum chloride (1.60 mg, 0.012 mmol) was dissolved in 0.2 M sodium acetate-acetic acid buffer (pH=4.6) (0.8 mL), and sodium fluoride (0.50 mg, 0.012 mmol) was added, and the reaction solution was stirred at room temperature for 5 minutes. Ethanol (0.60 mL) and compound 65 (8.09 mg, 0.01 mmol) were added, and the reaction solution was heated at 100 C. for 30 minutes. The reaction solution was cooled to room temperature, and directly purified by Pre-HPLC to obtain 66 (4.6 mg, yield: 53.93%).

Embodiment 67

##STR00205##

Synthesis of Compound 67-a

[0518] Compound 19-b (64.88 mg, 0.1 mmol), compound 59-b (54.02 mg, 0.130 mmol), and O-benzotriazole-tetramethyluronium hexafluorophosphate (75.85 mg, 0.200 mmol) were dissolved in N, N-dimethylformamide (1.0 mL), and diisopropylethylamine (0.050 mL, 0.30 mmol) was added, and the reaction solution was stirred at room temperature for 1 hour. The reaction solution was directly purified by Pre-HPLC to obtain 67-a (58 mg, yield: 55.43%).

Synthesis of Compound 67

[0519] Compound 67-a (58 mg, 0.055 mmol) was dissolved in dichloromethane (2 mL), and trifluoroacetic acid (2 mL) was added, and the reaction solution was stirred at room temperature for 24 hours. The reaction solution was directly purified by Pre-HPLC to obtain 67 (25 mg, yield: 41.10%).

[0520] .sup.1H NMR (400 MHz, MeOD) : 7.94 (s, 1H), 7.62 (d, J=15.8 Hz, 1H), 7.54 (t, J=3.4 Hz, 2H), 7.47-7.39 (m, 2H), 7.39-7.23 (m, 5H), 7.18 (d, J=7.5 Hz, 1H), 4.63-4.49 (m, 2H), 4.40 (d, J=13.3 Hz, 1H), 4.16 (d, J=6.3 Hz, 2H), 3.95 (d, J=12.7 Hz, 1H), 3.84-3.53 (m, 7H), 3.44-3.33 (m, 1H), 3.26-2.61 (m, 15H), 2.30 (s, 3H), 2.29-2.17 (m, 2H), 2.06-1.49 (m, 7H), 1.49-1.23 (m, 2H).

Embodiment 68

##STR00206##

Synthesis of Compound 68

[0521] Aluminum chloride (1.60 mg, 0.012 mmol) was dissolved in 0.2 M sodium acetate-acetic acid buffer (pH=4.6) (0.8 mL), and sodium fluoride (0.50 mg, 0.012 mmol) was added, and the reaction solution was stirred at room temperature for 5 minutes. Ethanol (0.60 mL) and compound 67 (8.78 mg, 0.01 mmol) were added, and the reaction solution was heated at 100 C. for 30 minutes. The reaction solution was cooled to room temperature, and directly purified by Pre-HPLC to obtain 68 (4.74 mg, yield: 51.41%).

Embodiment 69

##STR00207## ##STR00208##

Synthesis of Compound 69-a

[0522] 2-methylpropan-2-yl (2R)-1-{[2-({2-[(2-bromoethyl)oxy]ethyl}oxy)-4-[(1E)-2-(2-methyl-3-phenylphenyl)vinyl]-5-(trifluoromethyl)phenyl]methyl}hexahydropyridine-2-carboxylate (140.53 mg, 0.2 mmol) and compound tert-butyl 2,2,2-(1,4,7,10-tetraazacyclododecan-1,4,7-triyl)triacetate (154.41 mg, 0.300 mmol) were dissolved in acetonitrile (5.0 mL), and potassium carbonate (55.28 mg, 0.400 mmol) was added. The reactant was heated and stirred at 60 C. for 16 hours. The reaction solution was cooled to room temperature, filtered, and concentrated under reduced pressure to obtain 69-a (226 mg, yield: 99.43%), which was directly used in the next step of reaction without purification.

Synthesis of Compound 69

[0523] Compound 69-a (226 mg, 0.199 mmol) was dissolved in dichloromethane (3.0 mL), and trifluoroacetic acid (3.0 mL) was added, and the reaction solution was stirred at room temperature overnight, and directly separated by Pre-HPLC to obtain 69 (127 mg, yield: 70.02%).

Embodiment 70

##STR00209##

Synthesis of Compound 70

[0524] Compound 69 (13.68 mg, 0.015 mmol) and lutetium trichloride (8.44 mg, 0.030 mmol) were dissolved in 0.2 M AcONa/AcOH buffer (pH=4.5, 1.0 mL), and the reaction solution was stirred at room temperature for 1 hour. The reaction solution was directly purified by Prep-HPLC to obtain 70 (9.77 mg, yield: 60.09%). LC-MS (ESI): m/z=1084.68(M+H).sup.+.

Embodiment 71

##STR00210## ##STR00211##

Synthesis of Compound 71-a

[0525] Compound 53-b (180 mg, 0.259 mmol) and tert-butyl 2,2,2-(1,4,7,10-tetraazacyclododecan-1,4,7-triyl) triacetate (237.0 mg, 0.519 mmol) were dissolved in acetonitrile (30.0 mL), and potassium carbonate (35.81 mg, 0.259 mmol) was added. The reaction solution was heated and stirred at 60 C. for 3 hours, and the reaction solution was cooled to room temperature, concentrated under reduced pressure, and the residue was dissolved in dichloromethane (100 mL). The mixture was washed sequentially with water (50 ml2) and saturated brine (50 m1), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was purified by column chromatography (petroleum ether:ethyl acetate=10:1) to obtain 71-a (230 mg, yield: 75.13%). LC-MS (ESI): m/z=1080.5 (M+H).sup.+.

Synthesis of Compound 71

[0526] Compound 71-a (170 mg, 0.157 mmol) was dissolved in dichloromethane (15.0 mL), and trifluoroacetic acid (15.0 mL) was added, and the reaction solution was stirred at room temperature for 16 hours and concentrated under reduced pressure, and the residue was directly separated by pre-HPLC to obtain 71 (85.7 mg, yield: 63.6%). LC-MS (ESI): m/z=856.0(M+H).sup.+.

Embodiment 72

##STR00212##

[0527] Compound 71 (13.68 mg, 0.015 mmol) and lutetium trichloride (8.44 mg, 0.030 mmol) were dissolved in 0.2 M AcONa/AcOH buffer (pH=4.5, 1.0 mL), and the reaction solution was stirred at room temperature for 1 hour. The reaction solution was directly purified by prep-HPLC to obtain 72 (9.60 mg, yield: 53.3%). LC-MS (ESI): m/z=1028.02(M+H).sup.+.

Embodiment 73

##STR00213##

[0528] Compound 71 (11.0 mg, 0.013 mmol) and gallium trichloride (1.76 mg, 0.010 mmol) were added to water (0.2 mL), and the reaction solution was heated and stirred at 90 C. for 5 minutes. The reaction solution was cooled to room temperature, and the reaction solution was directly separated by Pre-HPLC to obtain 73 (11.1 mg, yield: 92.5%). LC-MS (ESI): m/z=922.77(M+H).sup.+.

Embodiment 74

##STR00214##

Synthesis of Compound 74

[0529] Compound 4 was dissolved in DMSO to a 10 mg/mL solution, and the solution was taken out a portion to dilute to 0.1 mg/mL with sodium acetate buffer which is metal-free and pH=5.5. The germanium-gallium generator was eluted with 5 mL of 0.1 M HCl in segments, and the highest activity portion (0.5 mL) was taken and 0.5 mL of sodium acetate buffer was added thereto, then 20-fold equivalent of compound 4 (0.1 mg/mL) was added. The mixture was vortexed and mixed for 10 s, and heated and shaken at 95 C. and 800 rpm for 30 minutes. The C18 cartridge was activated with ethanol, then eluted clean with pure water and eluted dry, and the solution after the reaction completed was passed through the C18 cartridge, and the C18 cartridge was eluted with pure water and eluted dry and then eluted with ethanol. TLC purity detection was carried out using 1% EDTA as a developing agent, and compound 4 labeled with .sup.68Ga was detected by TLC scanning, and its radiochemical purity was 99.67%.

[0530] Appropriate amounts of .sup.68Ga-labeled compound 4 and compound 8 were taken for HPLC characterization according to the following conditions, and chromatographic conditions were as follows: [0531] Mobile phase A: 0.1% TFA-H.sub.2O [0532] Mobile phase B: ACN [0533] Chromatographic column: Waters XBridge, 19*150 mm, 5 um [0534] Flow rate: 1 ml/min [0535] Method: Time: 0 min 25% B, 10 min 95% B

[0536] After HPLC characterization, the UV peak time of compound 8 and the radioactive peak time of compound 4 labeled with .sup.68Ga are both around 7:07 (mm:ss), indicating that the labeling of compound 4 by .sup.68Ga was successful (namely, compound 74), which was consistent with the results of TLC scanning.

Embodiment 75

##STR00215##

Synthesis of Compound 75

[0537] Compound 2 was dissolved in DMSO to a 10 mg/mL solution, and the solution was taken out a portion to dilute to 0.1 mg/mL with sodium acetate buffer which is metal-free and pH=5.5. The germanium-gallium generator was eluted with 5 mL of 0.1 M HCl in segments, and the highest activity portion (0.5 mL) was taken and 0.5 mL of sodium acetate buffer was added thereto, then 20-fold equivalent of compound 2 (0.1 mg/mL) was added. The mixture was vortexed and mixed for 10 s, and heated and shaken at 95 C. and 800 rpm for 30 minutes. The C18 cartridge was activated with ethanol, then eluted clean with pure water and eluted dry, and the solution after the reaction completed was passed through the C18 cartridge, and the C18 cartridge was eluted with pure water and eluted dry, and then eluted with ethanol. The compound 2 labeled with .sup.68Ga was detected by TLC scanning, and its radiochemical purity was 99.74%.

[0538] Appropriate amounts of .sup.68Ga-labeled compound 2 and compound 7 were taken for HPLC characterization according to the following conditions, and chromatographic conditions were as follows: [0539] Mobile phase A: 0.1% TFA-H.sub.2O [0540] Mobile phase B: ACN [0541] Chromatographic column: Waters XBridge, 19*150 mm, 5 um [0542] Flow rate: 1 ml/min

[0543] Method: Time: 0 min 25% B, 10 min 95% B

[0544] After HPLC characterization, the UV peak time of compound 7 and the radioactive peak time of compound 2 labeled with .sup.68Ga are both around 7:03 (mm:ss), indicating that the labeling of compound 2 by .sup.68Ga was successful (namely, compound 75), which was consistent with the resluts of TLC scanning.

Embodiment 76

##STR00216##

Synthesis of Compound 76

[0545] Compound 1 was dissolved in DMSO to a 10 mg/mL solution, and the solution was taken out a portion to dilute to 0.1 mg/mL with sodium acetate buffer which is metal-free and pH=5.5. The metal bath reactor was turned on and preheated to 25 C. A solution of 1 mCi (about 50 pmol) .sup.177LuCl.sub.3 was taken, and then a solution of compound 1 with 20-fold equivalent was added, and the solution was supplemented to 50 L via sodium acetate buffer, and the mixture was reacted at 25 C. and 800 rpm for 120 minutes. TLC purity detection was carried out using 1% EDTA as a developing agent, and compound 1 labeled with .sup.177Lu was detected by TLC scanning, and its radiochemical purity was 96.90%.

[0546] Appropriate amounts of compound 15 and .sup.177Lu-labeled compound 1 were taken for HPLC characterization according to the following conditions, and chromatographic conditions were as follows: [0547] Mobile phase A: 0.1% TFA-water; [0548] Mobile phase B: acetonitrile; [0549] Method: 25% B-95% B, 10 min, UV214 nm; [0550] Flow rate: 1 mL/min; [0551] Chromatographic column: Velch Xtimate C18, 4.6*150 mm, 5 m.

[0552] The .sup.175Lu-labeled compound 1 was characterized by HPLC and the peak time was confirmed to be 5.731 minutes.

[0553] The amount of .sup.177Lu-labeled compound 1 was so low that UV light could not be seen, so a tube of mobile phase was collected every 0.5 minute, and a total of 20 tubes were collected. The radioactivity count of each tube of mobile phase was detected, and the radioactivity count-time curve was drawn. Compared with the HPLC of compound 15, it could be found that the peak time of .sup.177Lu-labeled compound 1 was consistent with compound 15, indicating that .sup.177Lu-labeled compound 1 (namely, compound 76) was successfully prepared.

TABLE-US-00001 Time/min 0-0.5 0.5-1 1-1.5 1.5-2 2-2.5 0.5-3 3-3.5 3.5-4 4-4.5 4.5-5 Radioactivity 80 123 253 199 156 177 85 101 139 192 count Time/min 5-5.5 5.5-6 6-6.5 6.5-7 7-7.5 7.5-8 8-8.5 8.5-9 9-9.5 9.5-10 Radioactivity 2091 33721 3054 868 879 407 349 413 421 123 count

Embodiment 77

##STR00217##

Synthesis of Compound 77

[0554] Compound 2 was dissolved in DMSO to a 10 mg/mL solution, and the solution was taken out a portion to dilute to 0.1 mg/mL with sodium acetate buffer which is metal-free and pH=5.5. The metal bath reactor was turned on and preheated to 95 C. A solution of 1 mCi (about 50 pmol) .sup.177LuCl.sub.3 was taken, and then a solution of compound 2 with 20-fold equivalent was added, and the solution was supplemented to 50 L via sodium acetate buffer, and the mixture was reacted at 95 C. and 800 rpm for 30 minutes. TLC purity detection was carried out using 1% EDTA as a developing agent, and compound 2 labeled with .sup.177Lu was detected by TLC scanning, and its radiochemical purity reached 100%, which could meet the requirements for animal administration and no further purification was needed.

[0555] Appropriate amounts of compound 6 and .sup.177Lu-labeled compound 2 were taken for HPLC characterization according to the following conditions, and chromatographic conditions were as follows: [0556] Mobile phase A: 0.1% TFA-water; [0557] Mobile phase B: acetonitrile; [0558] Method: 25% B-95% B, 10 min, UV214 nm; [0559] Flow rate: 1 mL/min; [0560] Chromatographic column: Velch Xtimate C18, 4.6*150 mm, 5 m.

[0561] The .sup.175Lu-labeled compound 2 was characterized by HPLC and the peak time was confirmed to be 6.457 minutes.

[0562] The amount of .sup.177Lu-labeled compound 2 was so low that UV light could not be seen, so a tube of mobile phase was collected every 0.5 minute, and a total of 20 tubes were collected. The radioactivity count of each tube of mobile phase was detected, and the radioactivity count-time curve was drawn. Compared with the HPLC of .sup.175Lu-labeled compound 2, it could be found that the peak time of .sup.177Lu-labeled compound 2 was consistent with compound 6, indicating that .sup.177Lu-labeled compound 2 (namely, compound 77) was successfully prepared.

TABLE-US-00002 Time/min 0-0.5 0.5-1 1-1.5 1.5-2 2-2.5 0.5-3 3-3.5 3.5-4 4-4.5 4.5-5 Radioactivity 67 70 55 177 82 65 106 58 58 51 count Time/min 5-5.5 5.5-6 6-6.5 6.5-7 7-7.5 7.5-8 8-8.5 8.5-9 9-9.5 9.5-10 Radioactivity 92 134 25596 22183 1146 63 55 60 116 105 count

Embodiment 78

##STR00218##

Synthesis of Compound 78

[0563] Compound 4 was dissolved in DMSO to a 10 mg/mL solution, and the solution was taken out a portion to dilute to 0.1 mg/mL with sodium acetate buffer which is metal-free and pH=5.5. The metal bath reactor was turned on and preheated to 95 C. A solution of 1 mCi (about 50 pmol).sup.177LuCl.sub.3 was taken, and then compound 4 with 20-fold equivalent was added, and the solution was supplemented to 50 L via sodium acetate buffer, and the mixture was reacted at 95 C. and 800 rpm for 30 minutes. TLC purity detection was carried out using 1% EDTA as a developing agent, and compound 4 labeled with .sup.177Lu was detected by TLC scanning, and its radiochemical purity reached 100%, which could meet the requirements for animal administration and no further purification was needed.

[0564] Appropriate amounts of compound 5 and .sup.177Lu-labeled compound 4 were taken for HPLC characterization according to the following conditions, and chromatographic conditions were as follows: [0565] Mobile phase A: 0.1% TFA-water; [0566] Mobile phase B: acetonitrile; [0567] Method: 25% B-95% B, 10 min, UV214 nm; [0568] Flow rate: 1 mL/min; [0569] Chromatographic column: Velch Xtimate C18, 4.6*150 mm, 5 m.

[0570] The .sup.175Lu-labeled compound 4 was characterized by HPLC and the peak time was confirmed to be 6.690 minutes.

[0571] The amount of .sup.177Lu-labeled compound 4 was so low that UV light could not be seen, so a tube of mobile phase was collected every 0.5 minute, and a total of 20 tubes were collected. The radioactivity count of each tube of mobile phase was detected, and the radioactivity count-time curve was drawn. Compared with the HPLC of compound 5, it can be found that the peak time of .sup.177Lu-labeled compound 4 was consistent with compound 5, indicating that .sup.177Lu-labeled compound 4 (namely, compound 78) was successfully prepared.

TABLE-US-00003 Time/min 0-0.5 0.5-1 1-1.5 1.5-2 2-2.5 0.5-3 3-3.5 3.5-4 4-4.5 4.5-5 Radioactivity 70 46 59 74 80 203 92 95 296 240 count Time/min 5-5.5 5.5-6 6-6.5 6.5-7 7-7.5 7.5-8 8-8.5 8.5-9 9-9.5 9.5-10 Radioactivity 199 479 1399 27203 5134 129 115 109 86 96 count

Embodiment 79

##STR00219##

[0572] Buffer system: sodium acetate-acetic acid buffer solution with a pH of around 4.0 and a concentration of 0.5 M (freshly prepared).

[0573] QMA column activation: 5 mL of water, 5 mL of freshly prepared sodium acetate-acetic acid buffer solution with a pH of around 4.0 and a concentration of 0.5 M.

[0574] F-18 ion purification: the QMA column was passed through target water and eluted sequentially with 0.3 mL buffer.

[0575] Precursor solution: 100 L buffer, 6 L AlCl.sub.3 buffer solution with a concentration of 10 mM, 300 L acetonitrile (reaction-promoting solvent), 20 L precursor solution (3 mg/mL).

[0576] The precursor solution was mixed evenly and let stand to equilibrate for 5 minutes.

[0577] 300 L of QMA column eluent containing F-18 was added to the reaction solution.

[0578] The plastic centrifuge tube was sealed and heated for 15 minutes, and the heating temperature was 100 C.

[0579] C18 Light cartridge purification: the reaction solution was diluted with 5 mL of water, then the sample was loaded to the C18 Light cartridge, and the product was eluted with 1 mL of ethanol-water solution at a concentration of 50% (v/v). The eluent was injected into HPLC for analysis.

[0580] The chromatographic conditions were as follows

TABLE-US-00004 Chromatographic Phenomenex, Luna 5C18(2) 110 A, 150 4.60 mm column: Detection 300 nm wavelength: Flow rate 1 mL/min; 0.1% TFA aqueous Time/min Acetonitrile solution Mobile phase: 0 40 60 3 70 30 10 70 30 12 40 60 15 40 60

[0581] Quality control analysis of compound 79

[0582] The radiochemical purity of compound 79 is 95.28%.

Embodiment 80

##STR00220##

[0583] Buffer system: sodium acetate-acetic acid buffer solution with a pH of around 4.0 and a concentration of 0.5 M (freshly prepared).

[0584] Compound 67 was dissolved in buffer solution, and 300 L of .sup.68Ga.sup.3+ solution was added. The plastic centrifuge tube was sealed and heated for 15 minutes, and the heating temperature was 100 C.

[0585] C18 Light cartridge purification: the reaction solution was diluted with 5 mL of water, then the sample was loaded to the C18 Light cartridge, and the product was eluted with 1 mL of ethanol-water solution at a concentration of 50% (v/v) to obtain compound 80.

Embodiment 81

##STR00221## ##STR00222##

Synthesis of Compound 81-h

[0586] Methyl 4-methoxypyridinecarboxylate (5000 mg, 29.94 mmol) was added to concentrated sulfuric acid (100 mL), and N-bromosuccinimide (7993.98 mg, 44.91 mmol) was added in batches at room temperature, and the reaction solution was stirred at room temperature for 16 hours. The reaction solution was cooled to 0 C., and then the reaction solution was slowly added into ice water (1.0 L), and the pH of the mixture was adjusted to 7-9 with saturated aqueous sodium bicarbonate. The mixture was extracted with ethyl acetate (1.0 L), and the organic phase was collected, washed sequentially with water (500 mL3) and saturated brine (500 mL1), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was separated by column chromatography (petroleum ether:ethyl acetate=3:1) to obtain 81-h (7 g, yield: 95.04%). LC-MS (ESI): m/z=248.3(M+H).sup.+.

Synthesis of Compound 81-g

[0587] Compound 81-h (7.0 g, 28.448 mmol) and potassium trifluoro(vinyl)borate (5675.45 mg, 42.673 mmol) were dissolved in dioxane (60.0 mL) and water (6.0 mL), and 1,1-bis(diphenylphosphino)ferrocene dichloropalladium (2081.57 mg, 2.845 mmol) and potassium carbonate (11795.5 mg, 85.3 mmol) were added. The reaction solution was heated and stirred at 90 C. for 16 hours, and the reaction solution was cooled to room temperature and concentrated under reduced pressure, and the residue was separated by column chromatography (petroleum ether:ethyl acetate=5:1) to obtain 81-g (3.4 g, yield: 61.86%). LC-MS (ESI): m/z=194.22(M+H).sup.+.

Synthesis of Compound 81-f

[0588] Compound 81-g (966.0 mg, 5.0 mmol) and 3-bromo-2-methylphenyl-1-amine (1023.2 mg, 5.50 mmol) were dissolved in tetrahydrofuran (30 mL), and the reaction solution was cooled to 0 C., and sodium bis(trimethylsilyl)amide (6.5 mL, 1.0 M) was added dropwise to the reaction solution. After dropwise addition, the reaction solution was stirred at room temperature for 1 hour, and ammonium chloride aqueous solution (100 mL) was slowly added to the reaction solution to quench the reaction. The mixture was extracted with ethyl acetate (150 mL), and the organic phase was collected, washed sequentially with water (100 mL3) and saturated brine (100 mL1), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was separated by column chromatography (petroleum ether:ethyl acetate=10:1) to obtain 81-f (1.4 g, yield: 80.64%). LC-MS (ESI): m/z=349.3(M+H).sup.+.

Synthesis of Compound 81-e

[0589] Compound 81-f (850 mg, 2.448 mmol) and potassium osmate (90.09 mg, 0.245 mmol) were dissolved in dioxane (60 mL) and water (20 mL), and sodium periodate (1570.86 mg, 7.344 mmol) was added in batches, and the reaction solution was stirred at room temperature for 6 hours. The reaction solution was filtered, and the filter cake was washed with dioxane (50 mL), and the filter cake was purified by column chromatography (petroleum ether:ethyl acetate=5:1) to obtain 81-e (360 mg, yield: 42.11%). LC-MS (ESI): m/z=351.2(M+H).sup.+.

Synthesis of Compound 81-d

[0590] Compound 81-e (360 mg, 1.03 mmol) and compound 2-e (382.02 mg, 2.06 mmol) were dissolved in methanol (60.0 mL), and sodium cyanoborohydride (129.91 mg, 2.06 mmol) and acetic acid (129.90 mg, 2.16 mmol) were added, and the reaction solution was heated and stirred at 60 C. for 6 hours. The reaction solution was cooled to room temperature and concentrated under reduced pressure, and the residue was separated by column chromatography (petroleum ether:ethyl acetate=5:1) to obtain 81-d (280 mg, yield: 52.38%). LC-MS (ESI): m/z=520.3(M+H).sup.+.

Synthesis of Compound 81-c

[0591] Compound 81-d (280.0 mg, 0.54 mmol) and compound 40-d (487.2 mg, 0.81 mmol) were dissolved in dioxane (50.0 mL) and water (5.0 mL), and 1,1-bis(diphenylphosphino)ferrocene dichloropalladium (39.52 mg, 0.054 mmol) and potassium carbonate (223.9 mg, 1.62 mmol) were added, and the reaction solution was heated and stirred at 110 C. for 12 hours. The reaction solution was cooled to room temperature and concentrated under reduced pressure, and the residue was separated by column chromatography (petroleum ether:ethyl acetate=5:1) to obtain 81-c (210 mg, yield: 38.46%). LC-MS (ESI): m/z=913.53 (M+H).sup.+.

Synthesis of Compound 81-b

[0592] Compound 81-c (198 mg, 0.217 mmol) and 1-bromo-2-[(2-bromoethyl)oxy]ethane (150.8 mg, 0.651 mmol) were dissolved in N, N-dimethylformamide (50.0 mL), and potassium carbonate (89.77 mg, 0.651 mmol) was added, and the reaction solution was heated and stirred at 80 C. for 12 hours. The reaction solution was cooled to room temperature and concentrated under reduced pressure, and the residue was dissolved with dioxane (60 mL), and the mixture was washed sequentially with water (40 mL3) and saturated brine (40 mL1), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the residue was separated by column chromatography (petroleum ether:ethyl acetate=5:1) to obtain 81-b (70 mg, yield: 28.6%). LC-MS (ESI): m/z=1065.14(M+H).sup.+.

Synthesis of Compound 81-a

[0593] Compound 81-b (70 mg, 0.066 mmol) and compound 47-b (47.07 mg, 0.132 mmol) were dissolved in acetonitrile (10.0 mL), and potassium carbonate (36.37 mg, 0.263 mmol) was added, and the reaction solution was heated and stirred at 60 C. for 3 hours. The reaction solution was cooled to room temperature and concentrated under reduced pressure, and the residue was separated by column chromatography (dichloromethane:methanol=10:1) to obtain 81-a (80 mg, yield: 90.7%). LC-MS (ESI): m/z=1341.0(M+H).sup.+.

Synthesis of Compound 81

[0594] Compound 81-a (80 mg, 0.060 mmol) was dissolved in dichloromethane (10.0 mL), and trifluoroacetic acid (5.0 mL) was added, and the reaction solution was stirred at room temperature for 6 hours and concentrated under reduced pressure, and the residue was directly separated by pre-HPLC to obtain 81 (28 mg, yield: 42.04%). LC-MS (ESI): m/z=1116.64(M+H).sup.+.

Embodiment 82

##STR00223##

Synthesis of Compound 82

[0595] Compound 81 (8.0 mg, 0.007 mmol) was dissolved in ethanol (0.5 mL), and the [AlF].sup.2+ solution (0.016 mmol, 1.6 mL) was added, and the reaction solution was stirred at 100 C. for 1 hour. The reaction solution was cooled to room temperature, and directly separated by pre-HPLC to obtain 82 (4 mg, yield: 48.08%). LC-MS (ESI): m/z=1160.8(M+H).sup.+.

Effect Embodiment 1

[0596] Homogenouse Time-Resolved Fluorescence (HTRF) binding assay was used to detect the binding ability of the compound of the present disclosure to PD-1/PD-L1.

[0597] The purchased kit (CisBio, #64CUS000C-1) contains reagents required for experiments such as PD-1, PD-L1, anti-tag1-Eu, Anti-tag2-XL665, Dilute Buffer, and Detection Buffer.

Experimental Steps

[0598] 1. The compound was configured with 100% DMSO into 10 concentrations with a concentration gradient of 3 times. [0599] 2. The DMSO solution of the compound was added to Dilute Buffer solution, and the mixture was mixed well and transferred to a 96-well plate. [0600] 3. PD-L1 was diluted with Dilute Buffer solution and then added to the above 96-well plate. [0601] 4. PD-1 was diluted with Dilute Buffer solution and then added to the above 96-well plate, and incubated at room temperature for 30 minutes. [0602] 5. One part of anti-tag1-Eu and one part of Anti-tag2-XL665 were added to Detection Buffer solution, and the mixture was mixed well and transferred to the above 96-well plate. [0603] 6. The mixture in the 96-well plate was incubated at room temperature for 1 to 24 hours. [0604] 7. The HTRF values were read with Envision.

Experimental Results

[0605] The biological activity of the compounds of the present disclosure were determined by the above tests, and the results obtained are as follows (Table 1):

TABLE-US-00005 TABLE 1 IC.sub.50 values of PD-1/PD-L1 binding of some compounds in the present disclosure. Compound IC.sub.50 (nM) 2 1.29 3 3.16 4 0.8881 6 2.658 7 0.9691 8 0.5216 9 1.072 10 169.3 11 32.57 12 32.52 13 299.5 14 0.95 15 5.33 16 1.422 17 1.191 18 0.9012 19 0.869 20 1.012 21 3.741 22 5.029 23 0.8334 24 0.7852 25 16.17 26 33.21 27 13.61 28 0.5616 29 0.5711 30 9.217 31 0.6027 32 12.37 33 0.6012 34 0.4048 35 0.7659 36 0.5214 37 0.7292 38 1.134 48 0.8853 50 3.316 52 4.377 54 7.365 56 11.46 57 4.834 59 5.471 62 0.5288 64 0.7003 66 1.08 68 1.249 69 24.85 70 47.7 71 13.24 72 112.5

Effect Embodiment 2

[0606] 1. Inhibitory effect of compound 78 on tumor [0607] 1.1 Experimental animal information: tumor-bearing C57/BL6 mice; SPF grade; weight range: 17-20 g; Shanghai Qi'up Biomedical Technology Co., Ltd. [0608] 1.2 Experimental process

[0609] Ten tumor-bearing mice with tumor volumes of 10-100 mm.sup.3 were systematically and randomly divided into 2 groups according to tumor size, with 5 mice in each group, corresponding to PBS and compound 78 respectively. After anesthesia with isoflurane, tumor-bearing mice were injected into the tail vein with compound 78 with 45 MBq (approximately 1.2 mCi) per mouse and a volume of 0.2 mL. After administration, the tumor size and weight of the animals were measured periodically, and the tumor growth curve was drawn to understand the inhibitory effect of the drug on tumor.

1.3 Experimental Results

[0610] Experimental results show that compared with the control group, compound 78 has a very good therapeutic effects on inhibiting tumor growth. (see FIG. 1).

[0611] The experiments were operated according to the above, and the experimental results show that: the injection of compound 5, compound 6, compound 12, compound 13, compound 14, compound 15, compound 17, compound 20, compound 22, compound 24, compound 26, compound 32, compound 33, compound 38, compound 41, compound 44, compound 45, compound 46, compound 70, compound 72, compound 76, and compound 77 respectively also has very good therapeutic effects on inhibiting tumor growth.

Effect Embodiment 3

[0612] Tumor targeting study of compound 79 in Micro-PET/CT scanning 1. Experimental animal information: C57BL/6J mice, SPF grade; 15-21 g; model mouse construction: bilateral tumor [0613] Construction of bilateral tumor model mice [0614] Cell culture

[0615] Human-derived PD-L1 gene knock-in MC-38 cells (MC-38-hPD-L1 cells) were adherently cultured in vitro, and the culture conditions were DMEM medium plus 10% heat-inactivated fetal bovine serum and hygromycinB (final concentration was 100 L/mL), and the cells were cultured at 37 C. with 5% CO.sub.2. Subculture of 2-3 times a week. When the cells were in the exponential growth phase, the cells were harvested, counted, and the left side of the mice was inoculated subcutaneously.

[0616] Mouse-derived MC-38 cells were adherently cultured in vitro, and the culture conditions were DMEM medium plus 10% heat-inactivated fetal bovine serum, and the cells were cultured at 37 C. with 5% CO.sub.2. Subculture of 2-3 times a week. When the cells were in the exponential growth phase, the cells were collected, counted, and the right side of the mice was inoculated subcutaneously.

Inoculation of Tumor Cell

[0617] 100 L of 110.sup.6 MC-38-hPD-L1 cell suspension was inoculated subcutaneously on the left dorsal side of C57BL/6J mice. The same mice were subcutaneously inoculated with 100 L of 110.sup.6 MC-38 cell suspension on the right dorsal side on the second day. After inoculation, the mice were fed normally, and after a certain number of days, tumor-bearing mice with the volume of bilateral transplanted tumor in the range of 150 mm.sup.3350 mm.sup.3 were selected for test.

Experiment Procedure

[0618] After quality control, compound 79 was diluted with 10% ethanol in physiological saline, and the drug was extracted and injected into each animal through tail vein. The administration volume was 100 L/animal, and the administration dose was 100-200 Ci/animal. The study of Micro-PET/CT imaging was performed at 0.5 h, 1.5 h, 2.5 h, 3.5 h after injection of compound 79.

Experimental Results

[0619] The experimental results show that the left side of bilateral tumor mice scanned by compound 79 was MC38-PDL1 and the right side was MC38. The results show that the tumor uptake value on the left side is significantly higher than that on the right side, as shown in Table 2.

TABLE-US-00006 TABLE 2 The values of tumor target uptake (unit: ID %/g) Compound 79 bilateral tumor model Time MC-38 MC38-PDL1 30 min 0.75 1.3 90 min 0.3 0.65 150 min 0.07 0.54 210 min 0.06 0.66

[0620] The experiments were operated according to the above, and the experimental results show that: compound 48, compound 50, compound 52, compound 54, compound 56, compound 58, compound 60, compound 62, compound 64, compound 66, compound 68, and compound 82 were injected respectively for Micro-PET/CT imaging, and it can be found that the uptake value of the mouse left tumor (MC38-PDL1) is significantly higher than that of the mouse right tumor (MC38).

Effect Embodiment 4

[0621] Tumor targeting study of compound 80 in Micro-PET/CT scanning [0622] Experimental animal information: C57BL/6J mice, SPF grade; 15-21 g; [0623] Construction of Bilateral Tumor Model Mice: [0624] Cell Culture

[0625] Human-derived PD-L1 gene knock-in MC-38 cells (MC-38-hPD-L1 cells) were adherently cultured in vitro, and the culture conditions were DMEM medium plus 10% heat-inactivated fetal bovine serum and hygromycinB (final concentration was 100 L/mL), and the cells were cultured at 37 C. with 5% CO.sub.2. Subculture of 2-3 times a week. When the cells were in the exponential growth phase, the cells were harvested, counted, and the left side of the mice was inoculated subcutaneously.

[0626] Mouse-derived MC-38 cells were adherently cultured in vitro, and the culture conditions were DMEM medium plus 10% heat-inactivated fetal bovine serum, and the cells were cultured at 37 C. with 5% CO.sub.2. Subculture of 2-3 times a week. When the cells were in the exponential growth phase, the cells were collected, counted, and the right side of the mice was inoculated subcutaneously.

Inoculation of Tumor Cell

[0627] 100 L of 110.sup.6 MC-38-hPD-L1 cell suspension was inoculated subcutaneously on the left dorsal side of C57BL/6J mice. The same mice were subcutaneously inoculated with 100 L of 110.sup.6 MC-38 cell suspension on the right dorsal side on the second day. After inoculation, the mice were fed normally, and after a certain number of days, tumor-bearing mice with the volume of bilateral transplanted tumor in the range of 150 mm.sup.3350 mm.sup.3 were selected for test.

Experiment Procedure

[0628] After quality control, compound 80 was diluted with 10% ethanol in physiological saline, and the drug was extracted and injected into each animal through tail vein. The administration volume was 100 L/animal, and the administration dose was 100-200 Ci/animal. The study of Micro-PET/CT imaging was performed at 0.5 h, 1.5 h, 2.5 h, 3.5 h after injection of compound 80.

Experimental Results

[0629] The experimental results show that the uptake value of the left side tumor (MC38-PDL1) in the model mice scanned with compound 80 is significantly higher than that of the right side (MC-38), as shown in Table 3.

TABLE-US-00007 TABLE 3 The values of tumor target uptake (unit: ID %/g) Compound 80 bilateral tumor model Time MC-38 MC38-PDL1 30 min 0.98 2.6 90 min 1.2 2.8 150 min 0.74 2.2 210 min 0.46 2.3

[0630] The experiments were operated according to the above, and the experimental results show that: compound 7, compound 8, compound 27, compound 28, compound 29, compound 34, compound 35, compound 36, compound 37, compound 73, compound 74, and compound 75 were injected respectively for Micro-PET/CT imaging, and it can be found that the uptake value of the mouse left tumor (MC38-PDL1) is significantly higher than that of the mouse right tumor (MC38).

[0631] Although specific embodiments of the present disclosure are described above, it should be understood by those skilled in the art that these are merely illustrative and that a variety of changes or modifications can be made to these embodiments without departing from the principles and substance of the present disclosure. Therefore, the scope of protection of the present disclosure is defined by the appended claims.