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PHENYL BENZYL ETHER DERIVATIVE AND PREPARATION METHOD AND APPLICATION THEREOF

20170037008 ยท 2017-02-09

    Inventors

    Cpc classification

    International classification

    Abstract

    Parts of compounds, after being labeled by radionuclide, of the phenyl benzyl ether derivative, are used as A plaque imaging agent. The structural formula of the phenyl benzyl ether derivative is shown by formula (I). The present invention develops a kind of brand new phenyl benzyl ether derivative which has high affinity with A plaques in brains of AD patients. The chemical structure of the phenyl benzyl ether derivative is different from that of compounds disclosed in the prior art and the phenyl benzyl ether derivative belongs to a brand new compound for diagnosing and treating AD. The obtained A plaque imaging agent has the advantages that the in-vivo stability is good, the fat solubility is low, the removal speed for the brain is fast, the problem of removing the radionuclide in vivo does not exist, and the application prospect and the market value are great.

    ##STR00001##

    Claims

    1-15. (canceled)

    16. A phenyl benzyl ether derivative having a structural formula shown by a formula (I): ##STR00012## wherein X is O, NH or S; Y.sub.1 and Y.sub.2 respectively and independently denote CH or nitrogen; R.sub.1 and R.sub.2 respectively and independently denote nitrogen, halogen, hydroxyl, hydrosulfuryl, alkoxy, alkyl, carbocyclic alkyl, heterocyclic alkyl, nitro, amino, alkylamino, cyan, carboxyl, aryl, heteraryl, arylalkoxy, substituted arylalkoxy, aryloxy, substituted aryloxy, arylalkenyl, substituted arylalkenyl, O(CH.sub.2)mNRaRb, CONRaRb, NHCORa, Sn (alkyl).sub.3, (CH.sub.2)m-Z, O(CH.sub.2)m-Z, (CH.sub.2)m- aryl or (OCH.sub.2CH.sub.2)n-Z; Ra and Rb respectively and independently denote hydrogen, alkyl or (CH.sub.2)m-aryl; Z denotes halogen, hydroxyl, trifluoromethylsulfonyl, methylsulfonyl or tolylsulfonyl; m and n are respectively integers from 1 to 6, preferably integers from 1 to 3 respectively.

    17. The phenyl benzyl ether derivative according to claim 16, wherein R.sub.1 and R.sub.2 are o-substituents, m-substituents or p-substituents.

    18. The phenyl benzyl ether derivative according to claim 16, wherein the halogen is fluorine, chlorine, bromine or iodine; the alkoxy is C.sub.1-C.sub.12 alkoxy, preferably C.sub.1-C.sub.6 alkoxy; the alkyl is C.sub.1-C.sub.12 alkyl, preferably C.sub.1-C.sub.6 alkyl; the carbocyclic alkyl is three-membered to six-membered carbocyclic alkyl, preferably cyclopropyl, cyclopentyl or cyclohexyl; heterocyclic alkyl is three-membered to six-membered heterocyclic alkyl, preferably piperidyl, piperazinyl or morpholine cyclic group; the alkylamino is C.sub.1-C.sub.12 alkylamino, preferably C.sub.1-C.sub.6 alkylamino, more preferably N-methylamino, dimethylamino, diethylamino, dipropylamino or diisopropylamino; the aryl is phenyl or naphthyl; the heteraryl is pyridyl, furyl, thienyl, benzothiazolyl, benzofuryl or benzoxazolyl; the arylalkoxy is C.sub.5-C.sub.7 aryl C.sub.1-C.sub.12 alkoxy, preferably phenylmethoxyl or phenylethyoxyl; the substituted arylalkoxy is substituted C.sub.5-C.sub.7 aryl C.sub.1-C.sub.12 alkoxy, preferably substituted phenylmethoxyl or substituted phenylethyoxyl; the aryloxy is C.sub.5-C.sub.7 aryloxy, preferably cyclopentadienyloxy or phenyloxy; the substituted aryloxy is substituted C.sub.5-C.sub.7 aryloxy, preferably substituted cyclopentadienyloxy or substituted phenyloxy; the arylalkenyl is C.sub.5-C.sub.7 aryl C.sub.2-C.sub.6 alkenyl, preferably phenylvinyl; and the substituted arylalkenyl is substituted C.sub.5-C.sub.7 aryl C.sub.2-C.sub.6 alkenyl, preferably substituted phenylvinyl.

    19. The phenyl benzyl ether derivative according to claim 17, wherein the halogen is fluorine, chlorine, bromine or iodine; the alkoxy is C.sub.1-C.sub.12 alkoxy, preferably C.sub.1-C.sub.6 alkoxy; the alkyl is C.sub.1-C.sub.12 alkyl, preferably C.sub.1-C.sub.6 alkyl; the carbocyclic alkyl is three-membered to six-membered carbocyclic alkyl, preferably cyclopropyl, cyclopentyl or cyclohexyl; heterocyclic alkyl is three-membered to six-membered heterocyclic alkyl, preferably piperidyl, piperazinyl or morpholine cyclic group; the alkylamino is C.sub.1-C.sub.12 alkylamino, preferably C.sub.1-C.sub.6 alkylamino, more preferably N-methylamino, dimethylamino, diethylamino, dipropylamino or diisopropylamino; the aryl is phenyl or naphthyl; the heteraryl is pyridyl, furyl, thienyl, benzothiazolyl, benzofuryl or benzoxazolyl; the arylalkoxy is C.sub.5-C.sub.7 aryl C.sub.1-C.sub.12 alkoxy, preferably phenylmethoxyl or phenylethyoxyl; the substituted arylalkoxy is substituted C.sub.5-C.sub.7 aryl C.sub.1-C.sub.12 alkoxy, preferably substituted phenylmethoxyl or substituted phenylethyoxyl; the aryloxy is C.sub.5-C.sub.7 aryloxy, preferably cyclopentadienyloxy or phenyloxy; the substituted aryloxy is substituted C.sub.5-C.sub.7 aryloxy, preferably substituted cyclopentadienyloxy or substituted phenyloxy; the arylalkenyl is C.sub.5-C.sub.7 aryl C.sub.2-C.sub.6 alkenyl, preferably phenylvinyl; and the substituted arylalkenyl is substituted C.sub.5-C.sub.7 aryl C.sub.2-C.sub.6 alkenyl, preferably substituted phenylvinyl.

    20. The phenyl benzyl ether derivative according to claim 16, wherein the structural formula is shown by a formula (I-1): ##STR00013## wherein X is O, NH or S; R.sub.1 is nitro, methoxy, hydroxyl, fluorine, chorine, bromine, iodine, hydrogen, tert-butyl, amino, methylamino, dimethylamino, OCH.sub.2CH.sub.2F, Sn(butyl).sub.3, OCH.sub.2CH.sub.2OH, (OCH.sub.2CH.sub.2).sub.3OH, OCH.sub.2CH.sub.2OTs, (OCH.sub.2CH.sub.2).sub.3OTs or (OCH.sub.2CH.sub.2).sub.3F; R.sub.2 is iodine, methoxy, bromine, hydrogen, OCH.sub.2CH.sub.2F, Sn(butyl).sub.3, OCH.sub.2CH.sub.2Br, OCH.sub.2CH.sub.2OTs or dimethylamino; preferably, R.sub.1 and R.sub.2 are respectively: TABLE-US-00010 R.sub.1 R.sub.2 Nitro Iodine Methoxy Iodine Hydroxyl Iodine Fluorine Iodine Chlorine Iodine Bromine Iodine Iodine Iodine Hydrogen Iodine Tert-butyl Iodine Amino Iodine Methylamino Iodine Dimethylamino Iodine Iodine Methoxy Methoxy Bromine Bromine Methoxy Dimethylamino Bromine OCH.sub.2CH.sub.2F Hydrogen OCH.sub.2CH.sub.2F Iodine OCH.sub.2CH.sub.2F Bromine Iodine OCH.sub.2CH.sub.2F Bromine OCH.sub.2CH.sub.2F Methoxy Sn(butyl).sub.3 Sn(butyl).sub.3 Methoxy Dimethylamino Sn(butyl).sub.3 OCH.sub.2CH.sub.2F Sn(butyl).sub.3 Sn(butyl).sub.3 OCH.sub.2CH.sub.2F Methoxy OCH.sub.2CH.sub.2F Methoxy OCH.sub.2CH.sub.2Br Nitro OCH.sub.2CH.sub.2F Amino OCH.sub.2CH.sub.2F Methylamino OCH.sub.2CH.sub.2F Dimethylamino OCH.sub.2CH.sub.2F Methoxy OCH.sub.2CH.sub.2OTs OCH.sub.2CH.sub.2OH Hydrogen (OCH.sub.2CH.sub.2).sub.3OH Hydrogen OCH.sub.2CH.sub.2OH Methoxy (OCH.sub.2CH.sub.2).sub.3OH Methoxy OCH.sub.2CH.sub.2OTs Methoxy (OCH.sub.2CH.sub.2).sub.3OTs Methoxy OCH.sub.2CH.sub.2F Methoxy (OCH.sub.2CH.sub.2).sub.3F Methoxy Iodine Dimethylamino and more preferably, R.sub.1, R.sub.2 and X are respectively: TABLE-US-00011 R.sub.1 R.sub.2 X p-OMe I O m-OMe I O o-OMe I O p-OH I O m-OH I O o-OH I O p-F I O p-Cl I O p-Br I O p-I I O P-H I O p-Bu.sup.t I O p-NH.sub.2 I O m-NH.sub.2 I O o-NH.sub.2 I O p-NHMe I O m-NHMe I O o-NHMe I O p-NMe.sub.2 I O m-NMe2 I O I P-OMe O p-OMe I S p-OCH.sub.2CH.sub.2F I O p-I OCH.sub.2CH.sub.2F O p-OMe OCH.sub.2CH.sub.2F O p-NHMe OCH.sub.2CH.sub.2F O p-NMe.sub.2 OCH.sub.2CH.sub.2F O p-OCH.sub.2CH.sub.2F OMe O P-(OCH.sub.2CH.sub.2).sub.3F OMe O p-I NMe.sub.2 NH

    21. The phenyl benzyl ether derivative according to claim 17, wherein the structural formula is shown by a formula (I-1): ##STR00014## wherein X is O, NH or S; R.sub.1 is nitro, methoxy, hydroxyl, fluorine, chorine, bromine, iodine, hydrogen, tert-butyl, amino, methylamino, dimethylamino, OCH.sub.2CH.sub.2F, Sn(butyl).sub.3, OCH.sub.2CH.sub.2OH, (OCH.sub.2CH.sub.2).sub.3OH, OCH.sub.2CH.sub.2OTs, (OCH.sub.2CH.sub.2).sub.3OTs or (OCH.sub.2CH.sub.2).sub.3F; R.sub.2 is iodine, methoxy, bromine, hydrogen, OCH.sub.2CH.sub.2F, Sn(butyl).sub.3, OCH.sub.2CH.sub.2Br, OCH.sub.2CH.sub.2OTs or dimethylamino; preferably, R.sub.1 and R.sub.2 are respectively: TABLE-US-00012 R.sub.1 R.sub.2 Nitro Iodine Methoxy Iodine Hydroxyl Iodine Fluorine Iodine Chlorine Iodine Bromine Iodine Iodine Iodine Hydrogen Iodine Tert-butyl Iodine Amino Iodine Methylamino Iodine Dimethylamino Iodine Iodine Methoxy Methoxy Bromine Bromine Methoxy Dimethylamino Bromine OCH.sub.2CH.sub.2F Hydrogen OCH.sub.2CH.sub.2F Iodine OCH.sub.2CH.sub.2F Bromine Iodine OCH.sub.2CH.sub.2F Bromine OCH.sub.2CH.sub.2F Methoxy Sn(butyl).sub.3 Sn(butyl).sub.3 Methoxy Dimethylamino Sn(butyl).sub.3 OCH.sub.2CH.sub.2F Sn(butyl).sub.3 Sn(butyl).sub.3 OCH.sub.2CH.sub.2F Methoxy OCH.sub.2CH.sub.2F Methoxy OCH.sub.2CH.sub.2Br Nitro OCH.sub.2CH.sub.2F Amino OCH.sub.2CH.sub.2F Methylamino OCH.sub.2CH.sub.2F Dimethylamino OCH.sub.2CH.sub.2F Methoxy OCH.sub.2CH.sub.2OTs OCH.sub.2CH.sub.2OH Hydrogen (OCH.sub.2CH.sub.2).sub.3OH Hydrogen OCH.sub.2CH.sub.2OH Methoxy (OCH.sub.2CH.sub.2).sub.3OH Methoxy OCH.sub.2CH.sub.2OTs Methoxy (OCH.sub.2CH.sub.2).sub.3OTs Methoxy OCH.sub.2CH.sub.2F Methoxy (OCH.sub.2CH.sub.2).sub.3F Methoxy Iodine Dimethylamino and more preferably, R.sub.1, R.sub.2 and X are respectively: TABLE-US-00013 R.sub.1 R.sub.2 X p-OMe I O m-OMe I O o-OMe I O p-OH I O m-OH I O o-OH I O p-F I O p-Cl I O p-Br I O p-I I O P-H I O p-Bu.sup.t I O p-NH.sub.2 I O m-NH.sub.2 I O o-NH.sub.2 I O p-NHMe I O m-NHMe I O o-NHMe I O p-NMe.sub.2 I O m-NMe2 I O I P-OMe O p-OMe I S p-OCH.sub.2CH.sub.2F I O p-I OCH.sub.2CH.sub.2F O p-OMe OCH.sub.2CH.sub.2F O p-NHMe OCH.sub.2CH.sub.2F O p-NMe.sub.2 OCH.sub.2CH.sub.2F O p-OCH.sub.2CH.sub.2F OMe O P-(OCH.sub.2CH.sub.2).sub.3F OMe O p-I NMe.sub.2 NH

    22. The phenyl benzyl ether derivative according to claim 18, wherein the structural formula is shown by a formula (I-1): ##STR00015## wherein X is O, NH or S; R.sub.1 is nitro, methoxy, hydroxyl, fluorine, chorine, bromine, iodine, hydrogen, tert-butyl, amino, methylamino, dimethylamino, OCH.sub.2CH.sub.2F, Sn(butyl).sub.3, OCH.sub.2CH.sub.2OH, (OCH.sub.2CH.sub.2).sub.3OH, OCH.sub.2CH.sub.2OTs, (OCH.sub.2CH.sub.2).sub.3OTs or (OCH.sub.2CH.sub.2).sub.3F; R.sub.2 is iodine, methoxy, bromine, hydrogen, OCH.sub.2CH.sub.2F, Sn(butyl).sub.3, OCH.sub.2CH.sub.2Br, OCH.sub.2CH.sub.2OTs or dimethylamino; preferably, R.sub.1 and R.sub.2 are respectively: TABLE-US-00014 R.sub.1 R.sub.2 Nitro Iodine Methoxy Iodine Hydroxyl Iodine Fluorine Iodine Chlorine Iodine Bromine Iodine Iodine Iodine Hydrogen Iodine Tert-butyl Iodine Amino Iodine Methylamino Iodine Dimethylamino Iodine Iodine Methoxy Methoxy Bromine Bromine Methoxy Dimethylamino Bromine OCH.sub.2CH.sub.2F Hydrogen OCH.sub.2CH.sub.2F Iodine OCH.sub.2CH.sub.2F Bromine Iodine OCH.sub.2CH.sub.2F Bromine OCH.sub.2CH.sub.2F Methoxy Sn(butyl).sub.3 Sn(butyl).sub.3 Methoxy Dimethylamino Sn(butyl).sub.3 OCH.sub.2CH.sub.2F Sn(butyl).sub.3 Sn(butyl).sub.3 OCH.sub.2CH.sub.2F Methoxy OCH.sub.2CH.sub.2F Methoxy OCH.sub.2CH.sub.2Br Nitro OCH.sub.2CH.sub.2F Amino OCH.sub.2CH.sub.2F Methylamino OCH.sub.2CH.sub.2F Dimethylamino OCH.sub.2CH.sub.2F Methoxy OCH.sub.2CH.sub.2OTs OCH.sub.2CH.sub.2OH Hydrogen (OCH.sub.2CH.sub.2).sub.3OH Hydrogen OCH.sub.2CH.sub.2OH Methoxy (OCH.sub.2CH.sub.2).sub.3OH Methoxy OCH.sub.2CH.sub.2OTs Methoxy (OCH.sub.2CH.sub.2).sub.3OTs Methoxy OCH.sub.2CH.sub.2F Methoxy (OCH.sub.2CH.sub.2).sub.3F Methoxy Iodine Dimethylamino and more preferably, R.sub.1, R.sub.2 and X are respectively: TABLE-US-00015 R.sub.1 R.sub.2 X p-OMe I O m-OMe I O o-OMe I O p-OH I O m-OH I O o-OH I O p-F I O p-Cl I O p-Br I O P-I I O P-H I O p-Bu.sup.t I O p-NH.sub.2 I O m-NH.sub.2 I O o-NH.sub.2 I O p-NHMe I O m-NHMe I O o-NHMe I O p-NMe.sub.2 I O m-NMe2 I O I P-OMe O p-OMe I S p-OCH.sub.2CH.sub.2F I O p-I OCH.sub.2CH.sub.2F O p-OMe OCH.sub.2CH.sub.2F O p-NHMe OCH.sub.2CH.sub.2F O p-NMe.sub.2 OCH.sub.2CH.sub.2F O p-OCH.sub.2CH.sub.2F OMe O P-(OCH.sub.2CH.sub.2).sub.3F OMe O p-I NMe.sub.2 NH

    23. The phenyl benzyl ether derivative according to claim 19, wherein the structural formula is shown by a formula (I-1): ##STR00016## wherein X is O, NH or S; R.sub.1 is nitro, methoxy, hydroxyl, fluorine, chorine, bromine, iodine, hydrogen, tert-butyl, amino, methylamino, dimethylamino, OCH.sub.2CH.sub.2F, Sn(butyl).sub.3, OCH.sub.2CH.sub.2OH, (OCH.sub.2CH.sub.2).sub.3OH, OCH.sub.2CH.sub.2OTs, (OCH.sub.2CH.sub.2).sub.3OTs or (OCH.sub.2CH.sub.2).sub.3F; R.sub.2 is iodine, methoxy, bromine, hydrogen, OCH.sub.2CH.sub.2F, Sn(butyl).sub.3, OCH.sub.2CH.sub.2Br, OCH.sub.2CH.sub.2OTs or dimethylamino; preferably, R.sub.1 and R.sub.2 are respectively: TABLE-US-00016 R.sub.1 R.sub.2 Nitro Iodine Methoxy Iodine Hydroxyl Iodine Fluorine Iodine Chlorine Iodine Bromine Iodine Iodine Iodine Hydrogen Iodine Tert-butyl Iodine Amino Iodine Methylamino Iodine Dimethylamino Iodine Iodine Methoxy Methoxy Bromine Bromine Methoxy Dimethylamino Bromine OCH.sub.2CH.sub.2F Hydrogen OCH.sub.2CH.sub.2F Iodine OCH.sub.2CH.sub.2F Bromine Iodine OCH.sub.2CH.sub.2F Bromine OCH.sub.2CH.sub.2F Methoxy Sn(butyl).sub.3 Sn(butyl).sub.3 Methoxy Dimethylamino Sn(butyl).sub.3 OCH.sub.2CH.sub.2F Sn(butyl).sub.3 Sn(butyl).sub.3 OCH.sub.2CH.sub.2F Methoxy OCH.sub.2CH.sub.2F Methoxy OCH.sub.2CH.sub.2Br Nitro OCH.sub.2CH.sub.2F Amino OCH.sub.2CH.sub.2F Methylamino OCH.sub.2CH.sub.2F Dimethylamino OCH.sub.2CH.sub.2F Methoxy OCH.sub.2CH.sub.2OTs OCH.sub.2CH.sub.2OH Hydrogen (OCH.sub.2CH.sub.2).sub.3OH Hydrogen OCH.sub.2CH.sub.2OH Methoxy (OCH.sub.2CH.sub.2).sub.3OH Methoxy OCH.sub.2CH.sub.2OTs Methoxy (OCH.sub.2CH.sub.2).sub.3OTs Methoxy OCH.sub.2CH.sub.2F Methoxy (OCH.sub.2CH.sub.2).sub.3F Methoxy Iodine Dimethylamino and more preferably, R.sub.1, R.sub.2 and X are respectively: TABLE-US-00017 R.sub.1 R.sub.2 X p-OMe I O m-OMe I O o-OMe I O p-OH I O m-OH I O o-OH I O p-F I O p-Cl I O p-Br I O p-I I O P-H I O p-Bu.sup.t I O p-NH.sub.2 I O m-NH.sub.2 I O o-NH.sub.2 I O p-NHMe I O m-NHMe I O o-NHMe I O p-NMe.sub.2 I O m-NMe2 I O I P-OMe O p-OMe I S p-OCH.sub.2CH.sub.2F I O p-I OCH.sub.2CH.sub.2F O p-OMe OCH.sub.2CH.sub.2F O p-NHMe OCH.sub.2CH.sub.2F O p-NMe2 OCH.sub.2CH.sub.2F O p-OCH.sub.2CH.sub.2F OMe O P-(OCH.sub.2CH.sub.2).sub.3F OMe O p-I NMe.sub.2 NH

    24. The phenyl benzyl ether derivative according to claim 16, wherein the structural formula is shown by a formula (I-2): wherein X is O, NH or S; R.sub.1 is hydrogen, bromine, iodine, nitro, amino, methylamino or dimethylamino; R.sub.2 is iodine, methoxy or OCH.sub.2CH.sub.2F; preferably, R.sub.1 and R.sub.2 are respectively: TABLE-US-00018 R.sub.1 R.sub.2 Hydrogen Iodine Bromine Iodine Iodine Iodine Nitro Iodine Amino Iodine Methylamino Iodine Dimethylamino Iodine Iodine Methoxy Iodine OCH.sub.2CH.sub.2F and more preferably, R.sub.1, R.sub.2 and X are respectively: TABLE-US-00019 R.sub.1 R.sub.2 X p-H I O p-I I O

    25. The phenyl benzyl ether derivative according to claim 17, wherein the structural formula is shown by a formula (I-2): wherein X is O, NH or S; R.sub.1 is hydrogen, bromine, iodine, nitro, amino, methylamino or dimethylamino; R.sub.2 is iodine, methoxy or OCH.sub.2CH.sub.2F; preferably, R.sub.1 and R.sub.2 are respectively: TABLE-US-00020 R.sub.1 R.sub.2 Hydrogen Iodine Bromine Iodine Iodine Iodine Nitro Iodine Amino Iodine Methylamino Iodine Dimethylamino Iodine Iodine Methoxy Iodine OCH.sub.2CH.sub.2F and more preferably, R.sub.1, R.sub.2 and X are respectively: TABLE-US-00021 R.sub.1 R.sub.2 X p-H I O p-I I O

    26. The phenyl benzyl ether derivative according to claim 18, wherein the structural formula is shown by a formula (I-2): wherein X is O, NH or S; R.sub.1 is hydrogen, bromine, iodine, nitro, amino, methylamino or dimethylamino; R.sub.2 is iodine, methoxy or OCH.sub.2CH.sub.2F; preferably, R.sub.1 and R.sub.2 are respectively: TABLE-US-00022 R.sub.1 R.sub.2 Hydrogen Iodine Bromine Iodine Iodine Iodine Nitro Iodine Amino Iodine Methylamino Iodine Dimethylamino Iodine Iodine Methoxy Iodine OCH.sub.2CH.sub.2F and more preferably, R.sub.1, R.sub.2 and X are respectively: TABLE-US-00023 R.sub.1 R.sub.2 X p-H I O p-I I O

    27. The phenyl benzyl ether derivative according to claim 19, wherein the structural formula is shown by a formula (I-2): wherein X is O, NH or S; R.sub.1 is hydrogen, bromine, iodine, nitro, amino, methylamino or dimethylamino; R.sub.2 is iodine, methoxy or OCH.sub.2CH.sub.2F; preferably, R.sub.1 and R.sub.2 are respectively: TABLE-US-00024 R.sub.1 R.sub.2 Hydrogen Iodine Bromine Iodine Iodine Iodine Nitro Iodine Amino Iodine Methylamino Iodine Dimethylamino Iodine Iodine Methoxy Iodine OCH.sub.2CH.sub.2F and more preferably, R.sub.1, R.sub.2 and X are respectively: TABLE-US-00025 R.sub.1 R.sub.2 X p-H I O P-I I O

    28. The phenyl benzyl ether derivative according to claim 16, wherein the structural formula is shown by a formula (I-3): ##STR00017## wherein X is O, NH or S; R.sub.1 is chlorine, bromine or iodine; R.sub.2 is iodine, methoxy or OCH.sub.2CH.sub.2; preferably, R.sub.1 and R.sub.2 are respectively: TABLE-US-00026 R.sub.1 R.sub.2 Chlorine Iodine Bromine Iodine Iodine Iodine Iodine Methoxy Iodine OCH.sub.2CH.sub.2F and more preferably, R.sub.1, R.sub.2 and X are respectively: TABLE-US-00027 R.sub.1 R.sub.2 X p-Cl I O p-Br I O p-I I O p-I OCH.sub.2CH.sub.2F O

    29. The phenyl benzyl ether derivative according to claim 17, wherein the structural formula is shown by a formula (I-3): ##STR00018## wherein X is O, NH or S; R.sub.1 is chlorine, bromine or iodine; R.sub.2 is iodine, methoxy or OCH.sub.2CH.sub.2; preferably, R.sub.1 and R.sub.2 are respectively: TABLE-US-00028 R.sub.1 R.sub.2 Chlorine Iodine Bromine Iodine Iodine Iodine Iodine Methoxy Iodine OCH.sub.2CH.sub.2F and more preferably, R.sub.1, R.sub.2 and X are respectively: TABLE-US-00029 R.sub.1 R.sub.2 X p-Cl I O p-Br I O p-I I O p-I OCH.sub.2CH.sub.2F O

    30. The phenyl benzyl ether derivative according to claim 18, wherein the structural formula is shown by a formula (I-3): ##STR00019## wherein X is O, NH or S; R.sub.1 is chlorine, bromine or iodine; R.sub.2 is iodine, methoxy or OCH.sub.2CH.sub.2; preferably, R.sub.1 and R.sub.2 are respectively: TABLE-US-00030 R.sub.1 R.sub.2 Chlorine Iodine Bromine Iodine Iodine Iodine Iodine Methoxy Iodine OCH.sub.2CH.sub.2F and more preferably, R.sub.1, R.sub.2 and X are respectively: TABLE-US-00031 R.sub.1 R.sub.2 X p-Cl I O p-Br I O p-I I O p-I OCH.sub.2CH.sub.2F O

    31. The phenyl benzyl ether derivative according to claim 19, wherein the structural formula is shown by a formula (I-3): ##STR00020## wherein X is O, NH or S; R.sub.1 is chlorine, bromine or iodine; R.sub.2 is iodine, methoxy or OCH.sub.2CH.sub.2; preferably, R.sub.1 and R.sub.2 are respectively: TABLE-US-00032 R.sub.1 R.sub.2 Chlorine Iodine Bromine Iodine Iodine Iodine Iodine Methoxy Iodine OCH.sub.2CH.sub.2F and more preferably, R.sub.1, R.sub.2 and X are respectively: TABLE-US-00033 R.sub.1 R.sub.2 X p-Cl I O p-Br I O p-I I O p-I OCH.sub.2CH.sub.2F O

    32. The phenyl benzyl ether derivative according to claim 16, wherein when the phenyl benzyl ether derivative contains fluorine atoms, F is .sup.18F or .sup.19F; when the phenyl benzyl ether derivative contains iodine atoms, I is .sup.123I, .sup.124I, .sup.125I, .sup.127I or .sup.131I; and when the phenyl benzyl ether derivative contains methyl, methoxy, N-methylamino or dimethylamino, CH.sub.3 is .sup.11CH3, OCH.sub.3 is O.sup.11CH.sub.3, NHCH.sub.3 is NH.sup.11CH.sub.3, and N(CH.sub.3).sub.2 is N(.sup.11CH.sub.3).sub.2 or N(CH.sub.3)(.sup.11CH.sub.3).

    33. The phenyl benzyl ether derivative according to claim 17, wherein when the phenyl benzyl ether derivative contains fluorine atoms, F is .sup.18F or .sup.19F; when the phenyl benzyl ether derivative contains iodine atoms, I is .sup.123I, .sup.124I, .sup.125I, .sup.127I or .sup.131I; and when the phenyl benzyl ether derivative contains methyl, methoxy, N-methylamino or dimethylamino, CH.sub.3 is .sup.11CH3, OCH.sub.3 is O.sup.11CH.sub.3, NHCH.sub.3 is NH.sup.11CH.sub.3, and N(CH.sub.3).sub.2 is N(.sup.11CH.sub.3).sub.2 or N(CH.sub.3)(.sup.11CH.sub.3).

    34. The phenyl benzyl ether derivative according to claim 18, wherein when the phenyl benzyl ether derivative contains fluorine atoms, F is .sup.18F or .sup.19F; when the phenyl benzyl ether derivative contains iodine atoms, I is .sup.123I, .sup.124I, .sup.125I, .sup.127I or .sup.131I; and when the phenyl benzyl ether derivative contains methyl, methoxy, N-methylamino or dimethylamino, CH.sub.3 is .sup.11CH3, OCH.sub.3 is O.sup.11CH.sub.3, NHCH.sub.3 is NH.sup.11CH.sub.3, and N(CH.sub.3).sub.2 is N(.sup.11CH.sub.3).sub.2 or N(CH.sub.3)(.sup.11CH.sub.3).

    35. The phenyl benzyl ether derivative according to claim 19, wherein when the phenyl benzyl ether derivative contains fluorine atoms, F is .sup.18F or .sup.19F; when the phenyl benzyl ether derivative contains iodine atoms, I is .sup.123I, .sup.124I, .sup.125I, .sup.127I or .sup.131I; and when the phenyl benzyl ether derivative contains methyl, methoxy, N-methylamino or dimethylamino, CH.sub.3 is .sup.11CH3, OCH.sub.3 is O.sup.11CH.sub.3, NHCH.sub.3 is NH.sup.11CH.sub.3, and N(CH.sub.3).sub.2 is N(.sup.11CH.sub.3).sub.2 or N(CH.sub.3)(.sup.11CH.sub.3).

    36. The phenyl benzyl ether derivative according to claim 20, wherein when the phenyl benzyl ether derivative contains fluorine atoms, F is .sup.18F or .sup.19F; when the phenyl benzyl ether derivative contains iodine atoms, I is .sup.123I, .sup.124I, .sup.125I, .sup.127I or .sup.131I; and when the phenyl benzyl ether derivative contains methyl, methoxy, N-methylamino or dimethylamino, CH.sub.3 is .sup.11CH3, OCH.sub.3 is O.sup.11CH.sub.3, NHCH.sub.3 is NH.sup.11CH.sub.3, and N(CH.sub.3).sub.2 is N(.sup.11CH.sub.3).sub.2 or N(CH.sub.3)(.sup.11CH.sub.3).

    37. The phenyl benzyl ether derivative according to claim 21, wherein when the phenyl benzyl ether derivative contains fluorine atoms, F is .sup.18F or .sup.19F; when the phenyl benzyl ether derivative contains iodine atoms, I is .sup.123I, .sup.124I, .sup.125I, .sup.127I or .sup.131I; and when the phenyl benzyl ether derivative contains methyl, methoxy, N-methylamino or dimethylamino, CH.sub.3 is .sup.11CH3, OCH.sub.3 is O.sup.11CH.sub.3, NHCH.sub.3 is NH.sup.11CH.sub.3, and N(CH.sub.3).sub.2 is N(.sup.11CH.sub.3).sub.2 or N(CH.sub.3)(.sup.11CH.sub.3).

    38. The phenyl benzyl ether derivative according to claim 22, wherein when the phenyl benzyl ether derivative contains fluorine atoms, F is .sup.18F or .sup.19F; when the phenyl benzyl ether derivative contains iodine atoms, I is .sup.123I, .sup.124I, .sup.125I, .sup.127I or .sup.131I; and when the phenyl benzyl ether derivative contains methyl, methoxy, N-methylamino or dimethylamino, CH.sub.3 is .sup.11CH3, OCH.sub.3 is O.sup.11CH.sub.3, NHCH.sub.3 is NH.sup.11CH.sub.3, and N(CH.sub.3).sub.2 is N(.sup.11CH.sub.3).sub.2 or N(CH.sub.3)(.sup.11CH.sub.3).

    39. The phenyl benzyl ether derivative according to claim 23, wherein when the phenyl benzyl ether derivative contains fluorine atoms, F is .sup.18F or .sup.19F; when the phenyl benzyl ether derivative contains iodine atoms, I is .sup.123I, .sup.124I, .sup.125I, .sup.127I or .sup.131I; and when the phenyl benzyl ether derivative contains methyl, methoxy, N-methylamino or dimethylamino, CH.sub.3 is .sup.11CH3, OCH.sub.3 is O.sup.11CH.sub.3, NHCH.sub.3 is NH.sup.11CH.sub.3, and N(CH.sub.3).sub.2 is N(.sup.11CH.sub.3).sub.2 or N(CH.sub.3)(.sup.11CH.sub.3).

    40. The phenyl benzyl ether derivative according to claim 24, wherein when the phenyl benzyl ether derivative contains fluorine atoms, F is .sup.18F or .sup.19F; when the phenyl benzyl ether derivative contains iodine atoms, I is .sup.123I, .sup.124I, .sup.125I, .sup.127I or .sup.131I; and when the phenyl benzyl ether derivative contains methyl, methoxy, N-methylamino or dimethylamino, CH.sub.3 is .sup.11CH3, OCH.sub.3 is O.sup.11CH.sub.3, NHCH.sub.3 is NH.sup.11CH.sub.3, and N(CH.sub.3).sub.2 is N(.sup.11CH.sub.3).sub.2 or N(CH.sub.3)(.sup.11CH.sub.3).

    41. The phenyl benzyl ether derivative according to claim 25, wherein when the phenyl benzyl ether derivative contains fluorine atoms, F is .sup.18F or .sup.19F; when the phenyl benzyl ether derivative contains iodine atoms, I is .sup.123I, .sup.124I, .sup.125I, .sup.127I or .sup.131I; and when the phenyl benzyl ether derivative contains methyl, methoxy, N-methylamino or dimethylamino, CH.sub.3 is .sup.11CH3, OCH.sub.3 is O.sup.11CH.sub.3, NHCH.sub.3 is NH.sup.11CH.sub.3, and N(CH.sub.3).sub.2 is N(.sup.11CH.sub.3).sub.2 or N(CH.sub.3)(.sup.11CH.sub.3).

    42. The phenyl benzyl ether derivative according to claim 26, wherein when the phenyl benzyl ether derivative contains fluorine atoms, F is .sup.18F or .sup.19F; when the phenyl benzyl ether derivative contains iodine atoms, I is .sup.123I, .sup.124I, .sup.125I, .sup.127I or .sup.131I; and when the phenyl benzyl ether derivative contains methyl, methoxy, N-methylamino or dimethylamino, CH.sub.3 is .sup.11CH3, OCH.sub.3 is O.sup.11CH.sub.3, NHCH.sub.3 is NH.sup.11CH.sub.3, and N(CH.sub.3).sub.2 is N(.sup.11CH.sub.3).sub.2 or N(CH.sub.3)(.sup.11CH.sub.3).

    43. The phenyl benzyl ether derivative according to claim 27, wherein when the phenyl benzyl ether derivative contains fluorine atoms, F is .sup.18F or .sup.19F; when the phenyl benzyl ether derivative contains iodine atoms, I is .sup.123I, .sup.124I, .sup.125I, .sup.127I or .sup.131I; and when the phenyl benzyl ether derivative contains methyl, methoxy, N-methylamino or dimethylamino, CH.sub.3 is .sup.11CH3, OCH.sub.3 is O.sup.11CH.sub.3, NHCH.sub.3 is NH.sup.11CH.sub.3, and N(CH.sub.3).sub.2 is N(.sup.11CH.sub.3).sub.2 or N(CH.sub.3)(.sup.11CH.sub.3).

    44. The phenyl benzyl ether derivative according to claim 28, wherein when the phenyl benzyl ether derivative contains fluorine atoms, F is .sup.18F or .sup.19F; when the phenyl benzyl ether derivative contains iodine atoms, I is .sup.123I, .sup.124I, .sup.125I, .sup.127I or .sup.131I; and when the phenyl benzyl ether derivative contains methyl, methoxy, N-methylamino or dimethylamino, CH.sub.3 is .sup.11CH3, OCH.sub.3 is O.sup.11CH.sub.3, NHCH.sub.3 is NH.sup.11CH.sub.3, and N(CH.sub.3).sub.2 is N(.sup.11CH.sub.3).sub.2 or N(CH.sub.3)(.sup.11CH.sub.3).

    45. The phenyl benzyl ether derivative according to claim 29, wherein when the phenyl benzyl ether derivative contains fluorine atoms, F is .sup.18F or .sup.19F; when the phenyl benzyl ether derivative contains iodine atoms, I is .sup.123I, .sup.124I, .sup.125I, .sup.127I or .sup.131I; and when the phenyl benzyl ether derivative contains methyl, methoxy, N-methylamino or dimethylamino, CH.sub.3 is .sup.11CH3, OCH.sub.3 is O.sup.11CH.sub.3, NHCH.sub.3 is NH.sup.11CH.sub.3, and N(CH.sub.3).sub.2 is N(.sup.11CH.sub.3).sub.2 or N(CH.sub.3)(.sup.11CH.sub.3).

    46. The phenyl benzyl ether derivative according to claim 30, wherein when the phenyl benzyl ether derivative contains fluorine atoms, F is .sup.18F or .sup.19F; when the phenyl benzyl ether derivative contains iodine atoms, I is .sup.123I, .sup.124I, .sup.125I, .sup.127I or .sup.131I; and when the phenyl benzyl ether derivative contains methyl, methoxy, N-methylamino or dimethylamino, CH.sub.3 is .sup.11CH3, OCH.sub.3 is O.sup.11CH.sub.3, NHCH.sub.3 is NH.sup.11CH.sub.3, and N(CH.sub.3).sub.2 is N(.sup.11CH.sub.3).sub.2 or N(CH.sub.3)(.sup.11CH.sub.3).

    47. The phenyl benzyl ether derivative according to claim 31, wherein when the phenyl benzyl ether derivative contains fluorine atoms, F is .sup.18F or .sup.19F; when the phenyl benzyl ether derivative contains iodine atoms, I is .sup.123I, .sup.124I, .sup.125I, .sup.127I or .sup.131I; and when the phenyl benzyl ether derivative contains methyl, methoxy, N-methylamino or dimethylamino, CH.sub.3 is .sup.11CH3, OCH.sub.3 is O.sup.11CH.sub.3, NHCH.sub.3 is NH.sup.11CH.sub.3, and N(CH.sub.3).sub.2 is N(.sup.11CH.sub.3).sub.2 or N(CH.sub.3)(.sup.11CH.sub.3).

    48. A preparation method of a phenyl benzyl ether derivative, wherein a reaction equation is: ##STR00021## wherein Y.sub.3 is bromine or chlorine; and R.sub.1, R.sub.2, X, Y.sub.1 and Y.sub.2 are correspondingly defined as that in the phenyl benzyl ether derivative shown by a structural formula such as a formula (I).

    49. A preparation method of a phenyl benzyl ether derivative, wherein a reaction equation is: ##STR00022## wherein Y.sub.3 is bromine or chlorine; R.sub.1, R.sub.2 and X are correspondingly defined as that in the phenyl benzyl ether derivative shown by a structural formula such as a formula (I-1).

    50. A preparation method of a phenyl benzyl ether derivative, wherein a reaction equation is: ##STR00023## wherein Y.sub.3 is bromine or chlorine; R.sub.1, R.sub.2 and X are correspondingly defined as that in the phenyl benzyl ether derivative shown by a structural formula such as a formula (I-2).

    51. A preparation method of a phenyl benzyl ether derivative, wherein a reaction equation is: ##STR00024## wherein Y.sub.3 is bromine or chlorine; R.sub.1, R.sub.2 and X are correspondingly defined as that in the phenyl benzyl ether derivative shown by a structural formula such as a formula (I-3).

    52. An A plaque imaging agent prepared by using a phenyl benzyl ether derivative, wherein, when the phenyl benzyl ether derivative contains fluorine atoms, prepared compounds containing F-18 are used as the A plaque imaging agent, especially a positron emission tomography (PET) A plaque imaging agent; or when the phenyl benzyl ether derivative contains iodine atoms, prepared compounds containing I-124 are used as the A plaque imaging agent, especially the PET A plaque imaging agent; or when the phenyl benzyl ether derivative contains methyl, methoxy, N-methylamino or dimethylamino, prepared compounds containing C-11 are used as the A plaque imaging agent, especially the PET A plaque imaging agent; or when the phenyl benzyl ether derivative contains iodine atoms, prepared compounds containing I-123, I-125 or I-131 are used as the A plaque imaging agent, especially a single photon emission computed tomography (SPECT) A plaque imaging agent.

    53. The A plaque imaging agent according to claim 52, wherein the A plaque imaging agent is a single photon or positron A plaque imaging agent.

    54. A method for preparation of a medicine for diagnosing an amyloidosis disease, comprising applying an A plaque imaging agent.

    55. A method for preparation of a medicine for diagnosing and treating an Alzheimer's disease, comprising applying a phenyl benzyl ether derivative.

    Description

    BRIEF DESCRIPTION OF THE DRAWINGS

    [0099] FIG. 1 is a reaction route diagram of a part 1 of an embodiment 1 and an embodiment 5.

    [0100] FIG. 2 is a reaction route diagram of a part 2 of the embodiment 1 and the embodiment 5.

    [0101] FIG. 3 is a reaction route diagram of an embodiment 3.

    [0102] FIG. 4 is a reaction route diagram of an embodiment 4.

    [0103] FIG. 5 and FIG. 6 are display images of autoradiography experiments in an embodiment 2.

    DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

    [0104] The following embodiments are used for describing the present invention instead of limiting the scope of the present invention.

    [0105] Operations which are not mentioned in the present invention are conventional operations in the field.

    [0106] [.sup.125I] NaI solution used in the present invention is bought from China Isotope & Radiation Corporation.

    [0107] Other materials used in the present invention are conventional materials which can be bought from the market or can be prepared by adopting the existing methods (for example, 4-hydroxy-N,N-dimethylaniline).

    [0108] A Room temperature in the present invention is 25 C.

    [0109] Concentration (%) of each material in the present invention is mass concentration.

    Embodiment 1

    Synthesis of Iodo Compounds

    [0110] A synthesis reaction route is shown in FIG. 1. Serial numbers of compounds in the embodiment 1 are consistent with serial numbers in the reaction route in FIG. 1.

    [0111] In the synthesis route shown in FIG. 1, reagents and conditions are as follows: (a) K.sub.2CO.sub.3, DME, 90 C.; (b) SnCl.sub.2.2H.sub.2O, EtOH, HCl, reflux; (c) 1:NaoMe, (CH.sub.2O).sub.n, MeOH, reflux; 2: NaBH.sub.4, reflux; (d) (CH.sub.2O).sub.n, NaBH.sub.3CN, HAc, r. t.; (e) 1-bromo-fluoroethane, KOH, ethanol, reflux; (f)10% Pd/C, latmH.sub.2, 50 C.; (g) NaBH.sub.4, MeOH, 0 C.; (h) PBr.sub.3, CH.sub.2Cl.sub.2, r. t.; (i) (Bu.sub.3Sn).sub.2, (PPh.sub.3).sub.4Pd, methylbenzene, Et.sub.3N, reflux; (j) [.sup.125I] NaI, HCl (1M), H.sub.2O.sub.2 (3%).

    1) Synthesis of 1-iodo-4-((4-nitrophenoxy) methyl) benzene (a compound 1)

    [0112] 4-nitrophenol (2.78 g, 20 mmol) and 4-iodobenzyl bromide (5.00 g, 20 mmol) are dissolved in 5 ml of anhydrous DMF, and K.sub.2CO.sub.3 (5.53 g, 40 mmol) is added. Reaction is conducted for 5 h at 90 C. under a reflux and stirring state, reaction is monitored through TLC till completion, depressurization is conducted to remove solvent, 50 ml of deionized water is added, white precipitate is separated out, suction filtration is conducted, the precipitate is washed with water and methanol recrystallization is conducted to obtain white solid 1 (1.69 g, 95.2%). HPLC: 7.51 min, 99.8%; mp 147.4-148.1 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 8.21 (d, J=9.2 Hz, 2H), 7.75 (d, J=8.3 Hz, 2H), 7.18 (d, J=8.3 Hz, 2H), 7.01 (d, J=9.2 Hz, 2H), 5.10 (s, 2H).

    2) Synthesis of 1-(4-iodobenzyloxy)-3-nitrobenzene (a compound 2)

    [0113] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 3-nitrophenol) to obtain white solid 2 (345.5 mg, 97.3%). HPLC: 8.53 min, 99.9%; mp 75.2-75.9 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 7.85 (d, J=8.0 Hz, 1H), 7.80 (s, 1H), 7.74 (d, J=8.2 Hz, 2H), 7.45 (t, J=8.2 Hz, 1H), 7.30-7.26 (m, 1H), 7.19 (d, J=8.1 Hz, 2H), 5.09 (s, 2H).

    3) Synthesis of 1-(4-iodobenzyloxy)-2-nitrobenzene (a compound 3)

    [0114] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 2-nitrophenol) to obtain yellow solid 3 (238.9 mg, 67.3%). HPLC: 6.03 min, 99.5%; mp 70.6-71.5 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 7.87 (dd, J=8.1, 1.4 Hz, 1H), 7.73 (d, J=8.2 Hz, 2H), 7.56-7.46 (m, 1H), 7.22 (d, J=8.1 Hz, 2H), 7.09-7.04 (m, 2H), 5.18 (s, 2H).

    4) Synthesis of 1-iodo-4-((4-methoxyphenoxy) methyl) benzene (a compound 4)

    [0115] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 4-methoxyphenol) to obtain white solid 4 (255.3 mg, 75.1%). HPLC: 8.28 min, 99.5%; mp 128.9-130.2 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 7.71 (d, J=8.2 Hz, 2H), 7.17 (d, J=8.2 Hz, 2H), 6.89 (d, J=9.2 Hz, 2H), 6.83 (d, J=9.2 Hz, 2H), 4.96 (s, 2H), 3.77 (s, 3H). .sup.13C NMR (101 MHz, CDCl.sub.3) 154.18, 152.68, 137.63, 137.08, 129.25, 115.92, 114.72, 93.30, 70.07, 55.72.

    5) Synthesis of 1-(4-iodobenzyloxy)-3-methoxybenzene (a compound 5)

    [0116] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 3-methoxyphenol) to obtain white solid 5 (211.7 mg, 62.2%). HPLC: 8.68 min, 98.5%; mp 77.4-78.7 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 7.71 (d, J=8.1 Hz, 2H), 7.21-7.17 (m, 3H), 6.57-6.50 (m, 2H), 4.99 (s, 2H), 3.79 (s, 3H).

    6) Synthesis of 1-(4-iodobenzyloxy)-2-methoxybenzene (a compound 6)

    [0117] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 2-methoxyphenol) to obtain white solid 6 (288.1 mg, 84.7%). HPLC: 6.63 min, 98.7%; mp 110.4-110.8 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 87.69 (d, J=8.1 Hz, 2H), 7.19 (d, J=8.0 Hz, 2H), 6.97-6.91 (m, 2H), 6.85 (d, J=3.8 Hz, 2H), 5.10 (s, 2H), 3.89 (s, 3H).

    7) Synthesis of 4-(4-iodobenzyloxy) phenol (a compound 7)

    [0118] P-dihydroxybenzene (110.1 mg, 1.0 mmol) and 4-iodobenzyl bromide (296.9 g, 1.0 mmol) are dissolved in 5 ml of anhydrous DMF, and K.sub.2CO.sub.3 (276.4 mg, 2.0 mmol) is added. Reaction is conducted for 2 h at 90 C. under a reflux and stirring state, reaction is monitored through TLC till completion, depressurization is conducted to remove solvent, 50 ml of deionized water is added, extraction is conducted by using CH.sub.2Cl.sub.2 (310 ml), organic phases are combined, drying is conducted by using anhydrous MgSO.sub.4, suction filtration is conducted, depressurization is conducted to remove solvent, and residues are separated through silica gel column chromatography (petroleum ether/ethyl acetate=4/1) to obtain white solid 7 (49.3 mg, 15.1%). HPLC: 3.75 min, 99.3%; mp 152.2-153.7 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 7.71 (d, J=8.3 Hz, 2H), 7.17 (d, J=8.2 Hz, 2H), 6.85-6.81 (m, 2H), 6.78-6.74 (m, 2H), 4.95 (s, 2H), 4.41 (s, 1H).

    8) Synthesis of 3-(4-iodobenzyloxy) phenol (a compound 8)

    [0119] Preparation is conducted according to the preparation method of the compound 7 (reactant p-dihydroxybenzene is replaced by m-dihydroxybenzene) to obtain white solid 8 (93.1 mg, 28.5%). HPLC: 3.95 min, 98.6%; mp 109.9-110.6 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 7.71 (d, J=7.9 Hz, 2H), 7.17 (d, J=8.2 Hz, 2H), 7.16-7.09 (m, 1H), 6.54 (d, J=8.6 Hz, 1H), 6.46-6.44 (m, 2H), 4.98 (s, 2H), 4.74 (s, 1H).

    9) Synthesis of 2-(4-iodobenzyloxy) phenol (a compound 9)

    [0120] Preparation is conducted according to the preparation method of the compound 7 (reactant p-dihydroxybenzene is replaced by o-dihydroxybenzene) to obtain white solid 9 (109.8 mg, 33.7%). HPLC: 4.25 min, 99.9%; mp 62.1-63.4 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 7.74 (d, J=8.2 Hz, 2H), 7.17 (d, J=8.0 Hz, 2H), 6.98-6.95 (m, 1H), 6.93-6.88 (m, 2H), 6.85-6.81 (m, 1H), 5.62 (s, 1H), 5.06 (s, 2H).

    10) Synthesis of 1-fluoro-4-(4-iodobenzyloxy) benzene (a compound 10)

    [0121] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 4-fluorophenol) to obtain white solid 10 (253.1 mg, 77.1%). HPLC: 8.92 min, 98.0%; mp 62.3-62.8 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 7.72 (d, J=8.2 Hz, 2H), 7.17 (d, J=8.2 Hz, 2H), 7.00-6.95 (m, 2H), 6.91-6.85 (m, 2H), 4.97 (s, 2H). [0148]

    11) Synthesis of 1-chloro-4-(4-iodobenzyloxy) benzene (a compound 11)

    [0122] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 4-chlorophenol) to obtain white solid 11 (136.2 mg, 79.0%). HPLC: 12.86 min, 99.6%; mp 107.5-108.1 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 7.72 (d, J=8.2 Hz, 2H), 7.24 (d, J=8.9 Hz, 2H), 7.16 (d, J=8.2 Hz, 2H), 6.87 (d, J=8.9 Hz, 2H), 4.98 (s, 2H).

    12) Synthesis of 1-bromo-4-(4-iodobenzyloxy) benzene (a compound 12)

    [0123] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 4-bromophenol) to obtain white solid 12 (302.5 mg, 77.8%). HPLC: 14.61 min, 99.3%; mp 122.6-123.5 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 7.71 (d, J=8.2 Hz, 2H), 7.37 (d, J=9.0 Hz, 2H), 7.16 (d, J=8.2 Hz, 2H), 6.82 (d, J=8.9 Hz, 2H), 4.97 (s, 2H).

    13) Synthesis of 1-iodo-4-(4-iodobenzyloxy) benzene (a compound 13)

    [0124] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 4-iodophenol) to obtain white solid 13 (436.0 mg, 89.3%). HPLC: 17.49 min, 98.2%; mp 135.0-135.9 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 7.71 (d, J=8.2 Hz, 2H), 7.56 (d, J=8.7 Hz, 2H), 7.15 (d, J=8.1 Hz, 2H), 6.72 (d, J=8.8 Hz, 2H), 4.97 (s, 2H).

    14) Synthesis of 1-iodo-4-(phenoxymethyl) benzene (a compound 14)

    [0125] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by phenol) to obtain white solid 14 (310.1 mg, 72.1%). HPLC: 9.59 min, 99.2%; mp 96.7-97.6 C; .sup.1H NMR (400 MHz, CDCl.sub.3) 7.72 (d, J=8.2 Hz, 2H), 7.32-7.27 (m, 2H), 7.19 (d, J=8.1 Hz, 2H), 6.99-6.94 (m, 3H), 5.02 (s, 2H).

    15) Synthesis of 1-tert-butyl-4-(4-iodobenzyloxy) benzene (a compound 15)

    [0126] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 4-tert-butylphenol) to obtain white solid 15 (366.2 mg, 87.4%). HPLC: 27.14 min, 98.3%; mp 91.9-93.0 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 7.71 (d, J=8.2 Hz, 2H, 7.31 (d, J=8.8 Hz, 2H), 7.18 (d, J=8.2 Hz, 2H), 6.89 (d, J=8.8 Hz, 2H), 4.99 (s, 2H), 1.30 (s, 9H).

    16) Synthesis of 4-(4-iodobenzyloxy) aniline (a compound 16)

    [0127] The compound 1 (1.42 g, 4.0 mmol) and SnCl.sub.2.2H.sub.2O (1.66 g, 8.0 mmol) are dissolved in 25 ml of ethanol, 2 ml of concentrated hydrochloric acid is dripped, reaction is conducted for 2 h at 80 C. under a reflux and stirring state, cooling to room temperature is conducted, 30 ml of 1M NaOH water solution is added to neutralize the hydrochloric acid and precipitate SnCl.sub.2, extraction is conducted by using ethyl acetate (310 ml), organic phases are combined, drying is conducted by using anhydrous MgSO.sub.4, suction filtration is conducted, depressurization is conducted to remove solvent, and residues are separated through silica gel column chromatography (petroleum ether/ethyl acetate=2/1) to obtain white solid 16 (643.3 mg, 49.5%). HPLC: 4.16 min, 98.4%; mp 138.6-140.0 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 7.70 (d, J=8.2 Hz, 2H), 7.16 (d, J=7.9 Hz, 2H), 6.78 (d, J=8.7 Hz, 2H), 6.64 (d, J=8.8 Hz, 2H), 4.93 (s, 2H), 3.44 (s, 2H).

    17) Synthesis of 3-(4-iodobenzyloxy) aniline (a compound 17)

    [0128] Preparation is conducted according to the preparation method of the compound 16 (reactant compound 1 is replaced by the compound 2) to obtain white solid 17 (695.5 mg, 73.1%). HPLC: 4.50 min, 99.4%; mp 153.9-154.8 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 7.70 (d, J=8.1 Hz, 2H), 7.17 (d, J=8.0 Hz, 2H), 7.07 (t, J=8.0 Hz, 1H), 6.40-6.34 (m, 3H), 4.97 (s, 2H).

    18) Synthesis of 2-(4-iodobenzyloxy) aniline (a compound 18)

    [0129] Preparation is conducted according to the preparation method of the compound 16 (reactant compound 1 is replaced by the compound 3) to obtain white solid 18 (99.3 mg, 11.4%). HPLC: 4.88 min, 99.1%; mp 99.1-100.1 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 7.71 (d, J=8.3 Hz, 2H), 7.19 (d, J=8.3 Hz, 2H), 6.85-6.78 (m, 3H), 6.75-6.71 (m, 1H), 5.03 (s, 2H).

    19) Synthesis of 4-(4-iodobenzyloxy)-N-methylaniline (a compound 19)

    [0130] The compound 16 (162.6 mg, 0.5 mmol) and paraformaldehyde (60.0 mg, 2.0 mmol) are dissolved in 30 ml of anhydrous methanol, 5 ml of NaOCH.sub.3 (54.0 mg, 1.0 mmol) methanol solution is added drop by drop, and reaction is conducted for 2 h under a reflux and stirring state. After cooling to room temperature is conducted, NaBH.sub.4 (75.6 mg, 2.0 mmol) is slowly added and continuously reaction is conducted for 2 h under a reflex and stirring state. Depressurization is conducted to remove solvent, 50 ml of 1M NaOH solution is added, white precipitate is separated out, suction filtration is conducted, the precipitate is washed with water, and methanol recrystallization is conducted to obtain pink solid 19 (152.4 mg, 89.9%). HPLC: 6.34 min, 99.2%; mp 93.9-95.2 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 7.70 (d, J=8.2 Hz, 2H), 7.17 (d, J=8.1 Hz, 2H), 6.84 (d, J=8.7 Hz, 2H), 6.58 (d, J=8.5 Hz, 2H), 4.94 (s, 2H), 2.81 (s, 3H).

    20) Synthesis of 3-(4-iodobenzyloxy)-N-methylaniline (a compound 20)

    [0131] The compound 17 (162.6 mg, 0.5 mmol) and paraformaldehyde (60.0 mg, 2.0 mmol) are dissolved in 30 ml of anhydrous methanol, 5 ml of NaOCH.sub.3 (54.0 mg, 1.0 mmol) methanol solution is added drop by drop, and reaction is conducted for 2 h under a reflux and stirring state. After cooling to room temperature is conducted, NaBH.sub.4 (75.6 mg, 2.0 mmol) is slowly added and continuously reaction is conducted for 2 h under a reflex and stirring state. Depressurization is conducted to remove solvent, 50 ml of 1M NaOH solution is added, extraction is conducted by using CH.sub.2Cl.sub.2 (310 ml), organic phases are combined, drying is conducted by using anhydrous MgSO.sub.4, suction filtration is conducted, depressurization is conducted to remove solvent, and residues are separated through silica gel column chromatography (petroleum ether/ethyl acetate=4/1) to obtain a colorless oily compound 20 (71.0 mg, 41.8%). HPLC: 6.60 min, 99.9%; mp 45.3-46.6 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 7.71 (d, J=8.1 Hz, 2H), 7.19 (d, J=8.0 Hz, 2H), 7.09 (t, J=8.0 Hz, 1H), 6.32 (d, J=8.0 Hz, 1H), 6.27 (d, J=7.9 Hz, 1H), 6.24 (s, 1H), 4.99 (s, 2H), 2.83 (s, 3H).

    21) Synthesis of 2-(4-iodobenzyloxy)-N-methylaniline (a compound 21)

    [0132] Preparation is conducted according to the preparation method of the compound 19 (reactant compound 16 is replaced by the compound 18), extraction is conducted by using CH.sub.2Cl.sub.2 (310 ml) after reaction is completed, organic phases are combined, drying is conducted by using anhydrous MgSO.sub.4, suction filtration is conducted, depressurization is conducted to remove solvent, and residues are separated through silica gel column chromatography (petroleum ether/ethyl acetate=4/1) to obtain a yellow oily compound 21 (34.2 mg, 67.2%). HPLC: 8.19 min, 98.1%; .sup.1H NMR (400 MHz, CDCl.sub.3) 7.72 (d, J=8.1 Hz, 2H), 7.19 (d, J=8.0 Hz, 2H), 6.94 (t, J=7.6 Hz, 1H), 6.80 (d, J=7.3 Hz, 1H), 6.72-6.64 (m, 2H), 5.02 (s, 2H), 2.87 (s, 3H).

    22) Synthesis of 4-(4-iodobenzyloxy)-N,N-dimethylaniline (a compound 22)

    [0133] The compound 16 (162.6 mg, 0.5 mmol) and paraformaldehyde (150.0 mg, 5.0 mmol) are dissolved in 20 ml of acetic acid, NaBH.sub.3CN (157.0 mg, 2.5 mmol) is slowly added, and reaction is conducted for 24 h at room temperature under a stirring state. 20 ml of 1M NaOH solution is added, white precipitate is separated out, suction filtration is conducted, the precipitate is washed with water and methanol recrystallization is conducted to obtain white solid 22 (168.4 mg, 95.4%). HPLC: 10.63 min, 98.4%; mp 128.2-129.3 C.; .sup.1H NMR (400 MHz, CDCl3) 7.69 (d, J=8.2 Hz, 2H), 7.17 (d, J=8.0 Hz, 2H), 6.88 (d, J=8.9 Hz, 2H), 6.82-6.68 (s, 2H), 4.95 (s, 2H), 2.87 (s, 6H).

    23) Synthesis of 3-(4-iodobenzyloxy)-N,N-dimethylaniline (a compound 23)

    [0134] Preparation is conducted according to the preparation method of the compound 22 (reactant compound 16 is replaced by the compound 17) to obtain white solid 23 (171.3 mg, 97.1%). HPLC: 11.30 min, 99.9%; mp 68.8-70.1 C.; 1H NMR (400 MHz, CDCl.sub.3) 7.71 (d, J=8.2 Hz, 2H), 7.19 (d, J=8.2 Hz, 2H), 7.15 (t, J=8.1 Hz, 1H), 6.43-6.30 (m, 3H), 5.00 (s, 2H), 2.94 (s, 6H). .sup.13C NMR (101 MHz, CDCl.sub.3) 150.92, 145.99, 137.59, 137.41, 129.28, 115.95, 114.77, 93.19, 70.16, 41.73.

    24) Synthesis of 1-iodo-4-(4-methoxybenzyloxy) benzene (a compound 24)

    [0135] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 4-iodophenol and reactant 4-iodobenzyl bromide is replaced by 4-methoxybenzyl bromide) to obtain white solid 24 (906.3 mg, 88.9%). HPLC: 8.55 min, 99.7%; mp 130.3-131.5 C.; 1H NMR (400 MHz, CDCl.sub.3) 7.55 (d, J=9.0 Hz, 2H), 7.33 (d, J=8.7 Hz, 2H), 6.91 (d, J=8.7 Hz, 2H), 6.74 (d, J=8.9 Hz, 2H), 4.95 (s, 2H), 3.81 (s, 3H). .sup.13C NMR (101 MHz, CDCl.sub.3) 159.59, 158.71, 138.22, 129.19, 128.55, 117.36, 114.08, 82.95, 69.91, 55.31.

    25) Synthesis of (4-iodobenzyl) (4-methoxyphenyl) sulfane (a compound 25)

    [0136] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 4-methoxythiophenol) to obtain white solid 25 (712.4 mg, 94.7%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.56 (d, J=8.3 Hz, 2H), 7.23 (d, J=8.8 Hz, 2H), 6.90 (d, J=8.3 Hz, 2H), 6.79 (d, J=8.8 Hz, 2H), 3.89 (s, 2H), 3.78 (s, 3H). .sup.13C NMR (101 MHz, CDCl.sub.3) 159.43, 138.01, 137.40, 134.36, 130.81, 125.45, 114.54, 92.31, 55.31, 40.77.

    26) Synthesis of 1-bromo-4-((4-methoxyphenoxy) methyl) benzene (a compound 26)

    [0137] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 4-methoxyphenol and reactant 4-iodobenzyl bromide is replaced by p-bromobenzyl bromide) to obtain white solid 26 (2.93 g, 93.2%). mp 105.3-106.7 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 7.51 (d, J=8.3 Hz, 2H), 7.30 (d, J=8.3 Hz, 2H), 6.89 (d, J=9.2 Hz, 2H), 6.83 (d, J=9.2 Hz, 2H), 4.97 (s, 2H), 3.77 (s, 3H).

    27) Synthesis of 1-bromo-4-(4-methoxybenzyloxy) benzene (a compound 27)

    [0138] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 4-bromophenol and reactant 4-iodobenzyl bromide is replaced by 4-methoxybenzyl bromide) to obtain white solid 27 (681.4 mg, 77.8%). mp 122.1-122.9 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 7.37 (d, J=9.0 Hz, 2H), 7.33 (d, J=8.7 Hz, 2H), 6.91 (d, J=8.7 Hz, 2H), 6.84 (d, J=9.0 Hz, 2H), 4.96 (s, 2H), 3.82 (s, 3H).

    28) Synthesis of 4-(4-bromobenzyloxy)-N,N-dimethylaniline (a compound 28)

    [0139] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 4-hydroxy-N,N-dimethylaniline and reactant 4-iodobenzyl bromide is replaced by p-bromobenzyl bromide) to obtain white solid 28 (303.5 mg, 99.1%). mp 125.8-127.1 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 7.52-7.48 (m, 2H), 7.32-7.28 (m, 2H), 6.92-6.85 (m, 2H), 6.76 (s, 2H), 4.96 (s, 2H), 2.88 (s, 6H).

    29) Synthesis of 1-(benzyloxy)-4-(2-fluoroethoxy) benzene (a compound 29)

    [0140] 4-benzyloxyphenol (2.00 g, 10.0 mmol) and KOH (0.56 g, 10.0 mmol) are dissolved in 30 ml of anhydrous ethanol, reflux is conducted for 30 min by heating at 80 C., 20 ml of 1-bromo-2-fluoroethane (1.52 g, 12.0 mmol) ethanol solution, continuously reaction is conducted for 1 h under a reflux and stirring state, reaction is monitored through TLC till basic completion, depressurization is conducted to remove solvent, 50 ml of 1M NaOH solution is added, white precipitate is separated out, suction filtration is conducted, the precipitate is washed with water and methanol recrystallization is conducted to obtain white crystal 29 (2.23 g, 90.4%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.46-7.28 (m, 5H), 6.91 (d, J=9.2 Hz, 2H), 6.86 (d, J=9.3 Hz, 2H), 5.02 (s, 2H), 4.81-4.64 (m, 2H), 4.22-4.10 (m, 2H).

    30) Synthesis of 4-(2-fluoroethoxy) phenol (a compound 30)

    [0141] The compound 29 (2.08 g, 8.44 mmol) is dissolved in 10 ml of anhydrous methanol, palladium-carbon catalyst (89.4 mg, 0.84 mmol) is added, reaction is conducted for 4 h at 50 C. under a stirring state under the condition of 1 atm H.sub.2, reaction is monitored through TLC till completion, suction filtration is conducted to remove the palladium-carbon catalyst, and depressurization is conducted to remove solvent to obtain white solid 30 (1.32 g, 57.4%). .sup.1H NMR (400 MHz, CDCl.sub.3) 6.83 (d, J=8.9 Hz, 2H), 6.77 (d, J=9.0 Hz, 2H), 4.80-4.64 (m, 2H), 4.42 (s, 1H), 4.23-4.09 (m, 2H).

    31) Synthesis of 1-(2-fluoroethoxy)-4-((4-iodobenzyl) oxy) benzene (a compound 31a)

    [0142] The compound 30 (468.5 mg, 3.0 mmol) and 4-iodobenzyl bromide (890.8 mg, 3.0 mmol) are dissolved in 5 ml of anhydrous DMF, and K.sub.2CO.sub.3 (414.6 mg, 3.0 mmol) is added. Reaction is conducted for 0.5 h at 90 C. under a reflux and stirring state, reaction is monitored through TLC till completion, depressurization is conducted to remove solvent, 50 ml of deionized water is added, white precipitate is separated out, suction filtration is conducted, the precipitate is washed with water, and methanol recrystallization is conducted to obtain white solid 31a (986.8 mg, 88.4%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.70 (d, J=8.3 Hz, 2H), 7.16 (d, J=8.2 Hz, 2H), 6.90-6.84 (m, 4H), 4.96 (s, 2H), 4.79-4.65 (m, 2H), 4.21-4.11 (m, 2H). .sup.13C NMR (101 MHz, CDCl.sub.3) 153.11, 152.93, 137.62, 136.94, 129.24, 115.89, 115.79, 93.35, 82.86, 81.17, 69.96, 67.97, 67.76.

    32) Synthesis of 1-bromo-4-((4-(2-fluoroethoxy) phenoxy) methyl) benzene (a compound 31b)

    [0143] Preparation is conducted according to the preparation method of the compound 31a (reactant 4-iodobenzyl bromide is replaced by p-bromobenzyl bromide) to obtain white solid 31b (1.55 g, 95.2%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.50 (d, J=8.4 Hz, 2H), 7.29 (d, J=8.4 Hz, 2H), 6.90-6.84 (m, 4H), 4.97 (s, 2H), 4.80-4.65 (m, 2H), 4.21-4.11 (m, 2H).

    33) Synthesis of 4-(2-fluoroethoxy) benzaldehyde (a compound 32)

    [0144] P-hydroxybenzaldehyde (2.44 g, 20 mmol) and 1-bromo-2-fluoroethane (2.54 g, 20 mmol) are dissolved in 5 ml of anhydrous DMF, and K.sub.2CO.sub.3 (5.53 g, 40 mmol) is added. Reaction is conducted for 2 h at 90 C. under a reflux and stirring state, reaction is monitored through TLC till completion, depressurization is conducted to remove solvent, 50 ml of deionized water is added, extraction is conducted by using ethyl acetate (310 ml), drying is conducted by using anhydrous MgSO.sub.4, suction filtration is conducted, and depressurization is conducted to remove solvent to obtain yellow oily liquid 32 (2.95 g, 87.8%). .sup.1H NMR (400 MHz, CDCl.sub.3) 9.90 (s, 1H), 7.86 (d, J=8.7 Hz, 2H), 7.04 (d, J=8.6 Hz, 2H), 4.88-4.71 (m, 2H), 4.37-4.24 (m, 2H).

    34) Synthesis of (4-(2-fluoroethoxy) phenyl) methanol (a compound 33)

    [0145] The compound 32 (2.95 g, 17.6 mmol) is dissolved in 10 ml of anhydrous methanol, NaBH.sub.4 (1.33 g, 35.2 mmol) is slowly added at 0 C. under a stirring state, continuously reaction is conducted for 0.5 h, reaction is monitored through TLC till completion, 10 ml of deionized water is added to quench the reaction, depressurization is conducted to remove methanol, a proper amount of 1M HCl is added to neutralize to pH=7, extraction is conducted by using CH.sub.2Cl.sub.2 (310 ml), organic phases are combined, drying is conducted by using anhydrous MgSO.sub.4, suction filtration is conducted, and depressurization is conducted to remove solvent to obtain yellow oily liquid 33 (2.73 g, 91.1%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.31 (d, J=8.5 Hz, 2H), 6.93 (d, J=8.5 Hz, 2H), 4.84-4.68 (m, 2H), 4.63 (s, 2H), 4.27-4.17 (m, 2H).

    35) Synthesis of 1-(bromomethyl)-4-(2-fluoroethoxy) benzene (a compound 34)

    [0146] The compound 33 (2.73 g, 16.0 mmol) is dissolved in 25 ml of anhydrous CH.sub.2Cl.sub.2, 25 ml of PBr.sub.3 (4.33 g, 16.0 mmol) CH.sub.2Cl.sub.2 solution is slowly added at room temperature under a stirring state, continuously reaction is conducted for 0.5 h, reaction is monitored through TLC till completion, 20 ml of deionized water is added to quench the reaction, then 1 g of NaHCO.sub.3 is added, stirring is continuously conducted for 0.5 h, extraction is conducted by using CH.sub.2Cl.sub.2 (310 ml), organic phases are combined, drying is conducted by using anhydrous MgSO.sub.4, suction filtration is conducted, and depressurization is conducted to remove solvent to obtain colorless oily liquid 34 (3.54 g, 95.0%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.33 (d, J=8.6 Hz, 2H), 6.89 (d, J=8.6 Hz, 2H), 4.84-4.68 (m, 2H), 4.50 (s, 2H), 4.27-4.16 (m, 2H).

    36) Synthesis of 1-(2-fluoroethoxy)-4-((4-iodophenoxy) methyl) benzene (a compound 35a)

    [0147] Preparation is conducted according to the preparation method of the compound 31a (reactant 4-iodobenzyl bromide is replaced by the compound 34 and reactant compound 30 is replaced by 4-iodophenol) to obtain white solid 35a (623.4 mg, 94.1%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.55 (d, J=8.9 Hz, 2H), 7.34 (d, J=8.6 Hz, 2H), 6.94 (d, J=8.6 Hz, 2H), 6.74 (d, J=8.9 Hz, 2H), 4.95 (s, 2H), 4.83-4.68 (m, 2H), 4.27-4.16 (m, 2H). .sup.13C NMR (101 MHz, CDCl.sub.3) 158.65, 158.39, 138.23, 129.24, 129.21, 117.34, 114.81, 83.00, 82.72, 81.03, 69.80, 67.31, 67.10.

    37) Synthesis of 1-bromo-4-((4-(2-fluoroethoxy) benzyl) oxy) benzene (a compound 35b)

    [0148] Preparation is conducted according to the preparation method of the compound 31a (reactant 4-iodobenzyl bromide is replaced by the compound 34 and reactant compound 30 is replaced by 4-bromophenol) to obtain white solid 35b (1.03 g, 76.1%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.35 (7.39-7.31, 4H), 6.94 (d, J=8.0 Hz, 2H), 6.84 (d, J=8.2 Hz, 2H), 4.96 (s, 2H), 4.76 (d, J=47.3 Hz, 2H), 4.22 (d, J=27.8 Hz, 2H).

    38) Synthesis of tributyl (4-((4-methoxyphenoxy) methyl) phenyl) stannane (a compound 36)

    [0149] The compound 26 (146.6 mg, 0.5 mmol), hexabutyldistannane (580.1 mg, 1.0 mmol) and Tetrakis (triphenylphosphine) palladium (57.8 mg, 0.05 mmol) are dissolved in 10 ml of methylbenzene (containing 1 ml of triethylamine), and reaction is conducted over a night under a reflux and stirring state. Depressurization is conducted to remove solvent, and residues are separated through silica gel column chromatography (petroleum ether/ethyl acetate=15/1) to obtain a colorless oily compound 36 (89.5 mg, 35.6%). .sup.1HNMR (400 MHz, CDCl.sub.3) 7.49 (d, J=7.9 Hz, 2H), 7.39 (d, J=7.8 Hz, 2H), 6.93 (d, J=9.1 Hz, 2H), 6.85 (d, J=9.1 Hz, 2H), 5.00 (s, 2H), 3.78 (s, 3H), 1.59-1.51 (m, 6H), 1.39-1.29 (m, 6H), 1.15-0.97 (m, 6H), 0.90 (t, J=7.3 Hz, 9H).

    39) Synthesis of tributyl (4-(4-methoxybenzyloxy) phenyl) stannane (a compound 37)

    [0150] Preparation is conducted according to the preparation method of the compound 36 (reactant compound 26 is replaced by the compound 27) to obtain a colorless oily compound 37 (75.0 mg, 29.8%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.40-7.32 (m, 3H), 7.31-7.27 (m, 1H), 6.99-6.95 (m, 2H), 6.91 (d, J=8.4 Hz, 2H), 4.98 (s, 2H), 3.82 (s, 3H), 1.69-1.60 (m, 6H), 1.41-1.30 (m, 12H), 0.92 (t, J=7.3 Hz, 9H).

    40) Synthesis of N,N-dimethyl-4-(4-(tributylstannyl) benzyloxy) aniline (a compound 38)

    [0151] Preparation is conducted according to the preparation method of the compound 36 (reactant compound 26 is replaced by the compound 28) to obtain a colorless oily compound 38 (56.2 mg, 21.8%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.47 (d, J=7.7 Hz, 2H), 7.39 (d, J=7.6 Hz, 2H), 6.92 (d, J=9.0 Hz, 2H), 6.76 (d, J=8.7 Hz, 2H), 4.98 (s, 2H), 2.87 (s, 6H), 1.58-1.49 (m, 6H), 1.38-1.28 (m, 12H), 0.89 (t, J=7.4 Hz, 9H).

    41) Synthesis of tributyl (4-((4-(2-fluoroethoxy) phenoxy) methyl) phenyl) stannane (a compound 39)

    [0152] Preparation is conducted according to the preparation method of the compound 36 (reactant compound 26 is replaced by the compound 31b) to obtain a colorless oily compound 39 (325.6 mg, 30.4%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.54-7.41 (m, 2H), 7.37 (d, J=7.8 Hz, 2H), 6.92 (d, J=9.3 Hz, 2H), 6.87 (d, J=9.3 Hz, 2H), 4.99 (s, 2H), 4.80-4.65 (m, 2H), 4.22-4.11 (m, 2H), 1.58-1.50 (m, 6H), 1.39-1.27 (m, 6H), 1.14-0.96 (m, 6H), 0.88 (t, J=7.3 Hz, 9H).

    42) Synthesis of tributyl (4-((4-(2-fluoroethoxy) benzyl) oxy) phenyl) stannane (a compound 40)

    [0153] Preparation is conducted according to the preparation method of the compound 36 (reactant compound 26 is replaced by the compound 35b) to obtain a colorless oily compound 40 (134.6 mg, 25.1%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.37 (d, J=8.7 Hz, 2H), 7.32-7.26 (m, 2H), 6.99-6.93 (m, 4H), 5.00 (s, 2H), 4.83-4.68 (m, 2H), 4.28-4.17 (m, 2H), 1.58-1.50 (m, 6H), 1.39-1.27 (m, 6H), 1.14-0.96 (m, 6H), 0.88 (t, J=7.3 Hz, 9H).

    Embodiment 2

    Synthesis of Fluoro Compounds

    [0154] A synthesis reaction route is shown in FIG. 2. Serial numbers of compounds in the embodiment 2 are consistent with serial numbers in the reaction route in FIG. 2.

    [0155] In the synthesis route shown in FIG. 2, reagents and conditions are as follows:

    [0156] (a) 1-bromo-2-fluoroethane or 1, 2-dibromoethane, K.sub.2CO.sub.3, DMF, 90 C.; (b) NaBH.sub.4, MeOH, 0 C.; (c) PBr.sub.3, CH.sub.2Cl.sub.2, r. t.; (d) 4-methoxyphenol or 4-nitrophenol, K.sub.2CO.sub.3, DMF, 90 C.; (e) SnCl.sub.2.2H.sub.2O, EtOH, HCl, reflux; (f) 1: Na0Me, (CH.sub.2O).sub.n, MeOH, reflux; 2: NaBH.sub.4, reflux; (g) (CH.sub.2O).sub.n, NaBH.sub.3CN, HAc, r.t.; (h) AgOTs, MeCN, reflux; (i) .sup.18F.sup., K.sub.2CO.sub.3, Kryptofix-2.2.2 (i.e., K.sub.222, aminopolyether), acetonitrile, 100 C.; (j) 2-chloroethanol or 2-(2-(2-chloroethoxy) ethoxy) ethanol), KOH, EtOH, reflux; (k) 10% Pd/C, 1 atm H.sub.2, 50 C.; (l) 1-(chloromethyl)-4-methoxybenzene (i.e., 4-methoxybenzyl chloride), K.sub.2CO.sub.3, DMF, 90 C.; (m) TsCl, CH.sub.2Cl.sub.2, Et.sub.3N, 0 C.-rt; (n) TBAF (1M in THF), THF, reflux.

    1) Synthesis of 4-(2-bromoethoxy) benzaldehyde (a compound 41)

    [0157] P-hydroxybenzaldehyde (2.44 g, 20 mmol) and 1, 2-dibromoethane (7.51 g, 40 mmol) are dissolved in 5 ml of anhydrous DMF, and K.sub.2CO.sub.3 (5.53 g, 40 mmol) is added. Reaction is conducted for 2 h at 90 C. under a reflux and stirring state, reaction is monitored through TLC till completion, depressurization is conducted to remove solvent, 50 ml of deionized water is added, extraction is conducted by using CH.sub.2Cl.sub.2 (310 ml), organic phases are combined, drying is conducted by using anhydrous MgSO.sub.4, suction filtration is conducted, depressurization is conducted to remove solvent, and residues are separated through silica gel column chromatography (petroleum ether/ethyl acetate=4/1) to obtain white solid 41 (1.32 g, 28.9%). .sup.1H NMR (400 MHz, CDCl.sub.3) 9.90 (s, 1H), 7.85 (d, J=8.8 Hz, 2H), 7.02 (d, J=8.7 Hz, 2H), 4.38 (t, J=6.2 Hz, 2H), 3.67 (t, J=6.2 Hz, 2H).

    2) Synthesis of (4-(2-bromoethoxy) phenyl) methanol (a compound 42)

    [0158] Preparation is conducted according to the preparation method of the compound 33 (reactant compound 32 is replaced by the compound 41) to obtain white solid 42 (1.14 g, 95.8%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.30 (d, J=8.5 Hz, 2H), 6.91 (d, J=8.6 Hz, 2H), 4.63 (s, 2H), 4.30 (t, J=6.3 Hz, 2H), 3.64 (t, J=6.3 Hz, 2H).

    3) Synthesis of 1-(2-bromoethoxy)-4-(bromomethyl) benzene (a compound 43)

    [0159] Preparation is conducted according to the preparation method of the compound 34 (reactant compound 33 is replaced by the compound 42) to obtain white solid 43 (1.29 g, 99.0%)..sup.1H NMR (400 MHz, CDCl.sub.3) 7.33 (d, J=8.7 Hz, 2H), 6.87 (d, J=8.7 Hz, 2H), 4.49 (s, 2H), 4.29 (t, J=6.3 Hz, 2H), 3.63 (t, J=6.3 Hz, 2H).

    4) Synthesis of 1-(2-fluoroethoxy)-4-((4-methoxyphenoxy) methyl) benzene (a compound 44a)

    [0160] The compound 34 (411.3 mg, 1.76 mmol) and 4-methoxyphenol (218.5 mg, 1.76 mmol) are dissolved in 5 ml of anhydrous DMF, and K.sub.2CO.sub.3 (243.2 mg, 1.76 mmol) is added. Reaction is conducted for 0.5 h at 90 C. under a reflux and stirring state, reaction is monitored through TLC till completion, depressurization is conducted to remove solvent, 50 ml of deionized water is added, white precipitate is separated out, suction filtration is conducted, the precipitate is washed with water and methanol recrystallization is conducted to obtain white solid 44a (136.5 mg, 28.1%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.35 (d, J=8.5 Hz, 2H), 6.97-6.87 (m, 4H), 6.83 (d, J=9.1 Hz, 2H), 4.94 (s, 2H), 4.84-4.67 (m, 2H), 4.28-4.15 (m, 2H), 3.77 (s, 3H). .sup.13C NMR (101 MHz, CDCl.sub.3) 158.24, 154.01, 152.99, 130.09, 129.20, 115.95, 114.74, 114.67, 82.74, 81.04, 70.45, 67.31, 67.10, 55.71.

    5) Synthesis of 1-(2-bromoethoxy)-4-((4-methoxyphenoxy) methyl) benzene (a compound 44b)

    [0161] Preparation is conducted according to the preparation method of the compound 44a (reactant compound 34 is replaced by the compound 43) to obtain white solid 44b (242.8 mg, 68.1%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.35 (d, J=8.6 Hz, 2H), 6.94-6.87 (m, 4H), 6.83 (d, J=9.2 Hz, 2H), 4.94 (s, 2H), 4.30 (t, J=6.3 Hz, 2H), 3.77 (s, 3H), 3.63 (t, J=6.3 Hz, 2H).

    6) Synthesis of 1-(2-fluoroethoxy)-4-((4-nitrophenoxy) methyl) benzene (a compound 44c)

    [0162] Preparation is conducted according to the preparation method of the compound 44a (reactant 4-methoxyphenol is replaced by 4-nitrophenol) to obtain white solid 44c (2.35 g, 78.6%). .sup.1H NMR (400 MHz, CDCl.sub.3) 8.20 (d, J=9.2 Hz, 2H), 7.36 (d, J=8.5 Hz, 2H), 7.02 (d, J=9.2 Hz, 2H), 6.96 (d, J=8.5 Hz, 2H), 5.09 (s, 2H), 4.86-4.67 (m, 2H), 4.31-4.17 (m, 2H).

    7) Synthesis of 4-(4-(2-fluoroethoxy) benzyloxy) aniline (a compound 45)

    [0163] The compound 44c (1.94 g, 6.67 mmol) and SnCl.sub.2.2H.sub.2O (3.01 g, 13.34 mmol) are dissolved in 25 ml of ethanol, 2 ml of concentrated hydrochloric acid is dripped, reaction is conducted for 2 h at 80 C. under a reflux and stirring state, cooling to room temperature is conducted, 30 ml of 1M NaOH water solution is added to neutralize the hydrochloric acid and precipitate SnCl.sub.2, extraction is conducted by using ethyl acetate (310 ml), organic phases are combined, drying is conducted by using anhydrous MgSO.sub.4, suction filtration is conducted, and depressurization is conducted to remove solvent to obtain white solid 45 (1.26 g, 72.5%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.34 (d, J=8.4 Hz, 2H), 6.92 (d, J=8.5 Hz, 2H), 6.80 (d, J=8.6 Hz, 2H), 6.63 (d, J=8.6 Hz, 2H), 4.91 (s, 2H), 4.84-4.67 (m, 2H), 4.27-4.15 (m, 2H), 3.42 (s, 2H).

    8) Synthesis of 4-(4-(2-fluoroethoxy) benzyloxy)-N-methylaniline (a compound 46)

    [0164] The compound 45 (522.6 mg, 2.0 mmol) and paraformaldehyde(240.0 mg, 8.0 mmol) are dissolved in 30 ml of anhydrous methanol, 5 ml of NaOCH.sub.3 (216.1 mg, 4.0 mmol) methanol solution is added drop by drop, and reaction is conducted for 2 h under a reflux and stirring state. After cooling to room temperature is conducted, NaBH.sub.4 (302.4 mg, 8.0 mmol) is slowly added and continuously reaction is conducted for 2 h under a reflex and stirring state. Depressurization is conducted to remove solvent, 50 ml of 1M NaOH solution is added, white precipitate is separated out, suction filtration is conducted, the precipitate is washed with water, and methanol recrystallization is conducted to obtain light yellow crystal 46 (423.6 mg, 76.9%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.34 (d, J=4.8 Hz, 2H), 6.92 (d, J=4.8 Hz, 2H), 6.85 (d, J=5.0 Hz, 2H), 6.57 (d, J=4.9 Hz, 2H), 4.92 (s, 2H), 4.75 (d, J=47.4 Hz, 2H), 4.22 (d, J=27.6 Hz, 2H), 3.49 (s, 1H), 2.80 (s, 3H).

    9) Synthesis of 4-(4-(2-fluoroethoxy) benzyloxy)-N,N-dimethylaniline (a compound 47)

    [0165] The compound 45 (261.3 mg, 1.0 mmol) and paraformaldehyde (300.0 mg, 10.0 mmol) are dissolved in 20 ml of acetic acid, NaBH.sub.3CN (314.0 mg, 5.0 mmol) is slowly added and reaction is conducted for 24 h at room temperature under a stirring state. 20 ml of 1M NaOH solution is added, white precipitate is separated out, suction filtration is conducted, the precipitate is washed with water, and methanol recrystallization is conducted to obtain light yellow crystal 47 (213.9 mg, 75.8%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.35 (d, J=8.0 Hz, 2H), 6.96-6.87 (m, 4H), 6.77 (s, 2H), 4.94 (s, 2H), 4.75 (d, J=47.7 Hz, 2H), 4.22 (d, J=27.7 Hz, 2H), 2.88 (s, 6H).

    10) Synthesis of 2-(4-((4-methoxyphenoxy) methyl) phenoxy) ethyl-4-methylbenzenesulfonate (a compound 48)

    [0166] The compound 44b (137.2 mg, 0.41 mmol) and silver p-methylbenzene sulfonate (227.1 mg, 0.82 mg) are dissolved in 20 ml of acetonitrile, reaction is conducted for 12h at 90 C. under a reflux and stirring state, reaction is monitored through TLC till basic completion, depressurization is conducted to remove solvent, and residues are separated through silica gel column chromatography (petroleum ether/ethyl acetate=4/1) to obtain white solid 48 (174.4 mg, 60.6%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.82 (d, J=8.3 Hz, 2H), 7.34 (d, J=8.1 Hz, 2H), 7.31 (d, J=8.6 Hz, 2H), 6.89 (d, J=9.2 Hz, 2H), 6.82 (d, J=9.2 Hz, 2H), 6.78 (d, J=8.6 Hz, 2H), 4.92 (s, 2H), 4.39-4.35 (m, 2H), 4.17-4.13 (m, 2H), 3.77 (s, 3H), 2.45 (s, 3H). .sup.13C NMR (101 MHz, CDCl.sub.3) 157.80, 154.01, 152.94, 144.94, 132.96, 130.21, 129.86, 129.12, 127.99, 115.92 (overlapped), 114.66, 70.39, 68.09, 65.52, 55.72, 21.62.

    11) Synthesis of 2-(4-(benzyloxy) phenoxy) ethanol (a compound 49a)

    [0167] The 4-benzyloxyphenol (4.00 g, 20.0 mmol) and KOH (1.12 g, 20.0 mmol) are dissolved in 30 ml of anhydrous ethanol, reflux is conducted for 30 min by heating at 80 C., 20 ml of 2-chloroethanol (2.01 g, 25 mmol) ethanol solution, continuously reaction is conducted for 1 h under a reflux and stirring state, reaction is monitored through TLC till basic completion, depressurization is conducted to remove solvent, 50 ml of 1M NaOH solution is added, white precipitate is separated out, suction filtration is conducted, the precipitate is washed with water and methanol recrystallization is conducted to obtain white crystal 49a (2.35 g, 48.1%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.46-7.30 (m, 5H), 6.91 (d, J=9.1 Hz, 2H), 6.85 (d, J=9.0 Hz, 2H), 5.02 (s, 2H), 4.08-3.99 (m, 2H), 3.97-3.87 (m, 2H), 1.95 (s, 1H).

    12) Synthesis of 2-(2-(2-(4-(benzyloxy) phenoxy) ethoxy) ethoxy) ethanol (a compound 49b)

    [0168] Preparation is conducted according to the preparation method of the compound 49a (reactant 2-chloroethanol is replaced by 2-(2-(2-chloroethoxy) ethoxy) ethanol) to obtain white solid 49b (2.55 g, 38.3%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.46-7.29 (m, 5H), 6.93-6.81 (m, 4H), 5.01 (s, 2H), 4.12-4.02 (m, 2H), 3.86-3.79 (m, 2H), 3.75-3.67 (m, 6H), 3.64-3.59 (m, 2H), 2.16 (s, 1H).

    13) Synthesis of 4-(2-hydroxyethoxy) phenol (a compound 50a)

    [0169] The compound 49a (2.15 g, 8.79 mmol) is dissolved in 10 ml of anhydrous methanol, palladium-carbon catalyst (93.6 mg, 0.88 mmol) is added, reaction is conducted for 4 h at 50 C. under a stirring state under the condition ofl atm H.sub.2, reaction is monitored through TLC till completion, suction filtration is conducted to remove the palladium-carbon catalyst, and depressurization is conducted to remove solvent to obtain white solid 50a (1.35 g, 100%). .sup.1HNMR (400 MHz, DMSO) 8.86 (s, 1H), 6.74 (d, J=8.6 Hz, 2H), 6.66 (d, J=8.8 Hz, 2H), 4.78 (t, J=5.2 Hz, 1H), 3.90-3.80 (m, 2H), 3.70-3.61 (m, 2H).

    14) Synthesis of 4-(2-(2-(2-hydroxyethoxy) ethoxy) ethoxy) phenol (a compound 50b)

    [0170] Preparation is conducted according to the preparation method of the compound 50a (reactant compound 49a is replaced by the compound 49b) to obtain a colorless transparent oily compound 50b (1.78 g, 98.6%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.26 (s, 1H), 6.81-6.67 (m, 4H), 4.08-4.01 (m, 2H), 3.86-3.79 (m, 2H), 3.77-3.68 (m, 6H), 3.66-3.59 (m, 2H).

    15) Synthesis of 2-(4-(4-methoxybenzyloxy) phenoxy) ethanol (a compound 51a)

    [0171] The compound 50a (235.3 mg, 1.53 mmol) and 4-methoxybenzyl chloride (239.6 mg, 1.53 mmol) are dissolved in 5 ml of anhydrous DMF, and K.sub.2CO.sub.3 ((211.6 mg, 1.53 mmol) is added. Reaction is conducted for 0.5 h at 90 C. under a reflux and stirring state, reaction is monitored through TLC till completion, depressurization is conducted to remove solvent, deionized water is added, white precipitate is separated out, suction filtration is conducted, the precipitate is washed with water, and methanol recrystallization is conducted to obtain white solid 51a (282.8 mg, 67.4%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.34 (d, J=8.6 Hz, 2H), 6.94-6.82 (m, 6H), 4.94 (s, 2H), 4.06-4.01 (m, 2H), 3.96-3.90 (m, 2H), 3.81 (s, 3H).

    16) Synthesis of 2-(2-(2-(4-(4-methoxybenzyloxy) phenoxy) ethoxy) ethoxy) ethanol (a compound 51b)

    [0172] Preparation is conducted according to the preparation method of the compound 51a (reactant compound 50a is replaced by the compound 50b) to obtain white solid 51b (369.7 mg, 66.9%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.34 (d, J=8.0 Hz, 2H), 6.94-6.82 (m, 2H), 4.93 (s, 2H), 4.12-4.05 (m, 2H), 3.88-3.83 (m, 2H), 3.81 (s, 3H), 3.76-3.68 (m, 6H), 3.65-3.58 (m, 2H), 2.08 (s, 1H).

    17) Synthesis of 2-(4-(4-methoxybenzyloxy) phenoxy) ethyl-4-methylbenzenesulfonate (a compound 52a)

    [0173] The compound 51a (137.2 mg, 0.5 mmol) is dissolved in 10 ml of CH.sub.2Cl.sub.2, 10 ml of triethylamine is added, p-toluensulfonyl chloride (143.0 mg, 0.75 mmol) is slowly added under an ice-bath stirring state, continuously reaction is conducted for 4 h under a stirring state, reaction is monitored through TLC till completion, depressurization is conducted to remove solvent, 50 ml of deionized water is added, extraction is conducted by using CH.sub.2Cl.sub.2 (310 ml), drying is conducted by using anhydrous MgSO.sub.4, suction filtration is conducted, depressurization is conducted to remove solvent, and residues are separated through silica gel column chromatography (petroleum ether/ethyl acetate=4/1) to obtain white solid 52a (214.3 mg, 77.2%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.81 (d, J=8.1 Hz, 2H), 7.33 (d, J=8.1 Hz, 4H), 6.91 (d, J=8.4 Hz, 2H), 6.85 (d, J=8.7 Hz, 2H), 6.72 (d, J=8.9 Hz, 2H), 4.92 (s, 2H), 4.37-4.31 (m, 2H), 4.12-4.07 (m, 2H), 3.81 (s, 3H). .sup.13C NMR (101 MHz, CDCl.sub.3) 159.46, 153.57, 152.32, 144.89, 133.01, 129.84, 129.18, 128.00, 115.88, 115.76, 114.00, 70.45, 68.27, 66.26, 55.29, 21.62.

    18) Synthesis of 2-(2-(2-(4-(4 methoxybenzyloxy) phenoxy) ethoxy) ethoxy) ethyl-4-methylbenzenesulfonate (a compound 52b)

    [0174] Preparation is conducted according to the preparation method of the compound 52a (reactant compound 51a is replaced by the compound 51b) to obtain colorless transparent oily liquid 52b (225.4 mg, 83.9%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.79 (d, J=7.9 Hz, 2H), 7.37-7.30 (m, 4H), 6.93-6.82 (m, 6H), 4.93 (s, 2H), 4.19-4.13 (m, 2H), 4.08-4.02 (m, 2H), 3.83-3.76 (m, 5H), 3.71-3.58 (m, 6H), 2.43 (s, 3H). .sup.13C NMR (101 MHz, CDCl.sub.3) 159.44, 153.25, 153.12, 144.76, 133.17, 129.81, 129.36, 129.18, 127.96, 115.91, 115.66, 113.99, 70.81, 70.75, 70.52, 69.93, 69.25, 68.74, 68.13, 55.29, 21.59.

    19) Synthesis of 1-(2-fluoroethoxy)-4-(4 methoxybenzyloxy) benzene (a compound 53a)

    [0175] The compound 52a (128.6 mg, 0.3 mmol) is dissolved in 5 ml of anhydrous THF, 0.6 ml of tetrabutylammonium fluoride tetrahydrofuran solution (1M) is added. Reaction is conducted for 2 h at 80 C. under a reflux and stirring state, reaction is monitored through TLC till completion, depressurization is conducted to remove solvent, and residues are separated through silica gel column chromatography (petroleum ether/ethyl acetate=2/1) to obtain white solid 53a (70.7 mg, 85.3%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.34 (d, J=8.2 Hz, 2H), 6.94-6.84 (m, 6H), 4.94 (s, 2H), 4.81-4.64 (m, 2H), 4.23-4.11 (m, 2H), 3.81 (s, 3H). .sup.13C NMR (101 MHz, CDCl.sub.3) 159.48, 153.56, 152.80, 129.31, 129.19, 115.99, 115.82, 114.02, 82.90, 81.20, 70.52, 68.06, 67.85, 55.30.

    20) Synthesis of 1-(2-(2-(2-fluoroethoxy) ethoxy) ethoxy)-4-(4-methoxybenzyloxy) benzene (a compound 53b)

    [0176] Preparation is conducted according to the preparation method of the compound 53a (reactant compound 52a is replaced by the compound 52b) to obtain colorless transparent oily liquid 53b (87.5 mg, 73.7%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.34 (d, J=8.2 Hz, 2H), 6.94-6.82 (m, 4H), 4.93 (s, 2H), 4.56 (d, J=47.8 Hz, 2H), 4.09 (s, 2H), 3.85-3.70 (m, 11H). .sup.13C NMR (101 MHz, CDCl.sub.3) 159.42, 153.21, 153.13, 129.34, 129.18, 115.87, 115.64, 113.97, 83.97, 82.29, 70.85, 70.84, 70.54, 70.49, 70.34, 69.93, 68.12, 55.28.

    Embodiment 3

    Synthesis of Pyridine Derivatives

    [0177] A synthesis reaction route is shown in FIG. 3. Serial numbers of compounds in the embodiment 3 are consistent with serial numbers in the reaction route in FIG. 3.

    [0178] In the synthesis route shown in FIG. 3, reagents and conditions are as follows: (a) K.sub.2CO.sub.3, DNIF, 90 C.; (b) SnCl.sub.2.2H.sub.2O, EtOH, HCl, reflux; (c) CH.sub.3I, K.sub.2CO.sub.3, r.t.

    1) Synthesis of 2-((4-iodobenzyl) oxy) pyridine (a compound 54)

    [0179] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 2-hydroxypyridine) to obtain white solid 54 (187.5 mg, 60.3%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.67 (d, J=8.2 Hz, 2H), 7.34 (ddd, J=8.8, 6.7, 1.8 Hz, 1H), 7.26-7.24 (m, 1H), 7.06 (d, J=8.2 Hz, 3H), 6.66 (d, J=9.1 Hz, 1H), 6.19 (t, J=6.7 Hz, 1H), 5.09 (s, 2H).

    2) Synthesis of 2-chloro-5-((4-iodobenzyl) oxy) pyridine (a compound 55)

    [0180] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 2-chloro-5-hydroxypyridine) to obtain white solid 55 (635.7 mg, 92.0%). .sup.1H NMR (400 MHz, CDCl.sub.3) 8.11 (s, 1H), 7.73 (d, J=8.2 Hz, 2H), 7.24-7.21 (m, 2H), 7.16 (d, J=8.1 Hz, 2H), 5.04 (s, 2H).

    3) Synthesis of 5-bromo-2-((4-iodobenzyl) oxy) pyridine (a compound 56)

    [0181] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 5-bromo-2-hydroxypyridine) to obtain white solid 56 (346.5 mg, 88.8%). 1H NMR (400 MHz, CDCl.sub.3) 7.69 (d, J=8.3 Hz, 2H), 7.36-7.32 (m, 2H), 7.06 (d, J=8.2 Hz, 2H), 6.54 (d, J=10.5 Hz, 1H), 5.03 (s, 2H).

    4) Synthesis of 2-bromo-5-((4-iodobenzyl) oxy) pyridine (a compound 57)

    [0182] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 2-bromo-5-hydroxypyridine) to obtain white solid 57 (361.7 mg, 92.7%). .sup.1H NMR (400 MHz, CDCl.sub.3) 8.11 (d, J=3.1 Hz, 1H), 7.73 (d, J=8.2 Hz, 2H), 7.37 (d, J=8.7 Hz, 1H), 7.17-7.11 (m, 3H), 5.03 (s, 2H).

    5) Synthesis of 5-iodo-2-((4-iodobenzyl) oxy) pyridine (a compound 58)

    [0183] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 2-hydroxy-5-iodopyridine) to obtain white solid 58 (321.5 mg, 73.6%). .sup.1H NMR (400 MHz, CDCl3) 7.69 (d, J=8.3 Hz, 2H), 7.45 (d, J=2.2 Hz, 1H), 7.42 (dd, J=9.5, 2.4 Hz, 1H), 7.05 (d, J=8.2 Hz, 2H), 6.44 (d, J=9.5 Hz, 1H), 5.02 (s, 2H).

    6) Synthesis of 2-iodo-5-((4-iodobenzyl) oxy) pyridine (a compound 59)

    [0184] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 2-iodo-5-hydroxypyridine) to obtain white solid 59 (289.8 mg, 48.8%). .sup.1H NMR (400 MHz, CDCl.sub.3) 8.06-8.02 (m, 1H), 7.75 (d, J=8.2 Hz, 2H), 7.24 (d, J=8.4 Hz, 2H), 7.21-7.15 (m, 1H), 7.03-6.98 (m, 1H), 5.12 (s, 2H).

    7) Synthesis of 2-((4-iodobenzyl) oxy)-5-nitropyridine (a compound 60)

    [0185] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 2-hydroxy-5-nitropyridine) to obtain yellow solid 60 (343.0 mg, 96.3%). .sup.1H NMR (400 MHz, CDCl.sub.3) 8.58 (d, J=3.0 Hz, 1H), 8.08 (dd, J=10.1, 3.0 Hz, 1H), 7.73 (d, J=8.2 Hz, 2H), 7.11 (d, J=8.2 Hz, 2H), 6.60 (d, J=10.1 Hz, 1H), 5.12 (s, 2H).

    8) Synthesis of 6-((4-iodobenzyl) oxy) pyridin-3-amine (a compound 61)

    [0186] Preparation is conducted according to the preparation method of the compound 16 (reactant compound 1 is replaced by the compound 60) to obtain blue solid 61 (203.4 mg, 82.0%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.66 (d, J=8.2 Hz, 2H), 7.06-7.02 (m, 3H), 6.70 (d, J=2.9 Hz, 1H), 6.57 (d, J=9.6 Hz, 1H), 5.01 (s, 2H).

    9) Synthesis of 6-((4-iodobenzyl) oxy)-N,N-dimethylpyridin-3-amine (a compound 62)

    [0187] Preparation is conducted according to the preparation method of the compound 21 (reactant compound 18 is replaced by the compound 61) to obtain blue solid 62 (66.8 mg, 35.6%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.67 (d, J=8.3 Hz, 3H), 7.34 (d, J=9.7 Hz, 1H), 7.09 (d, J=8.0 Hz, 2H), 6.67 (d, J=9.8 Hz, 1H), 5.06 (s, 2H), 2.82 (s, 6H).

    10) Synthesis of 2-iodo-5-((4-methoxybenzyl) oxy) pyridine (a compound 63)

    [0188] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 2-iodo-5-hydroxypyridine and reactant 4-iodobenzyl bromide is replaced by 4-methoxybenzyl bromide) to obtain white solid 63 (569.1 mg, 83.4%). .sup.1H NMR (400 MHz, CDCl.sub.3) 8.01 (dd, J=4.6, 1.4 Hz, 1H), 7.39 (d, J=8.6 Hz, 2H), 7.16 (dd, J=8.1, 4.6 Hz, 1H), 7.05-7.01 (m, 1H), 6.93 (d, J=8.7 Hz, 2H), 5.11 (s, 2H), 3.82 (s, 3H).

    11) Synthesis of 5-iodo-2-((4-methoxybenzyl) oxy) pyridine (a compound 64)

    [0189] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 2-hydroxy-5-iodopyridine and reactant 4-iodobenzyl bromide is replaced by 4-methoxybenzyl bromide) to obtain white solid 64 (297.4 mg, 87.2%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.46 (d, J=2.4 Hz, 1H), 7.40 (dd, J=9.5, 2.4 Hz, 1H), 7.26 (d, J=8.6 Hz, 2H), 6.89 (d, J=8.6 Hz, 2H), 6.45 (d, J=9.5 Hz, 1H), 5.02 (s, 2H), 3.80 (s, 3H).

    12) Synthesis of 5-((4-(2-fluoroethoxy) benzyl) oxy)-2-iodopyridine (a compound 65)

    [0190] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 2-iodo-5-hydroxypyridine and reactant 4-iodobenzyl bromide is replaced by the compound 34) to obtain white solid 65 (357.4 mg, 73.1%). .sup.1H NMR (400 MHz, CDCl.sub.3) 8.05 (d, J=4.7 Hz, 1H), 7.40 (d, J=8.6 Hz, 2H), 7.21 (dd, J=8.0, 4.8 Hz, 1H), 7.07 (d, J=8.2 Hz, 1H), 6.96 (d, J=8.7 Hz, 2H), 5.13 (s, 2H), 4.85-4.68 (m, 2H), 4.29-4.18 (m, 2H).

    13) Synthesis of 2-((4-(2-fluoroethoxy) benzyl) oxy)-5-iodopyridine (a compound 66)

    [0191] Preparation is conducted according to the preparation method of the compound 1 (reactant 4-nitrophenol is replaced by 2-hydroxy-5-iodopyridine and reactant 4-iodobenzyl bromide is replaced by the compound 34) to obtain white solid 66 (297.8 mg, 79.8%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.47 (s, 1H), 7.43 (d, J=9.5 Hz, 1H), 7.29-7.26 (m, 2H), 6.92 (d, J=8.6 Hz, 2H), 6.51 (dd, J=9.4, 3.6 Hz, 1H), 5.04 (s, 2H), 4.83-4.68 (m, 2H), 4.27-4.15 (m, 2H).

    Embodiment 4

    Synthesis of Benzylamine Derivatives

    [0192] A synthesis reaction route is shown in FIG. 4. Serial numbers of compounds in the embodiment 4 are consistent with serial numbers in the reaction route in FIG. 4.

    [0193] In the synthesis route shown in FIG. 4, reagents and conditions are as follows: (a) EtOH, reflux; (b) NaBH.sub.4, MeOH, reflux.

    1) Synthesis of 4-(((4-iodophenyl) amino) methyl)-N,N-dimethylaniline (a compound 67)

    [0194] 4-iodoaniline (876.1 mg, 4.0 mmol) and 4-dimethylaminobenzaldehyde (596.8 mg, 4.0 mmol) are dissolved in 25 ml of anhydrous ethanol, reaction is conducted for 15 min at 90 C. under a reflux and stirring state, a great amount of white crystals are separated out, suction filtration is conducted after cooling, the crystals are washed with cold ethanol, the crystals are dried and then are dissolved in 50 ml of methanol, NaBH.sub.4 (453.6 mg, 12.0 mmol) is slowly added, and reaction is conducted for 30 min at 90 C. under a reflux and stirring state. Reaction is monitored through TLC till basic completion, depressurization is conducted to remove methanol, 50 ml of deionized water is added, a great amount of white solid is separated out, suction filtration is conducted, the solid is washed with water and drying is conducted to obtain a white solid product (821.1 mg, 58.3%). 1H NMR (400 MHz, CDCl.sub.3) 7.41 (d, J=8.5 Hz, 2H), 7.22 (d, J=8.1 Hz, 2H), 6.74 (s, 2H), 6.42 (d, J=8.6 Hz, 2H), 4.17 (s, 2H), 2.95 (s, 6H).

    Embodiment 5

    Preparation of .SUP.125.I and .SUP.18.F Labeled Ligands

    [0195] I. Experiment Steps:

    [0196] 1) Preparation of Compounds [.sup.125I] 4, [.sup.125I] 24, [.sup.125I] 22, [.sup.125I] 31a and [.sup.125I] 35a

    [0197] See FIG. 1 for the synthesis reaction route. 0.1 mg of each of corresponding tin precursors (respectively compounds 36, 37, 38, 39 and 40) is weighed and put in a glass reaction flask, 100 l of ethanol is added for dissolving, and then 1 l [.sup.125] NaI solution ((200 ci, 2200 Ci/mmol), 100 l of 1M hydrochloric acid and 50 l of H.sub.2O.sub.2 water solution (3%) are sequentially added. After sealing, reaction is conducted for 15 min at room temperature, 20 l of saturated sodium hydrogen sulfite is added to terminate reaction, and a proper amount of NaHCO.sub.3 is added to regulate pH to be neutral. Reaction liquid is separated through HPLC, separation conditions: Venusil MP C18 reversed phase column (5 m, 4.6250 mm); CH.sub.3CN:H.sub.2O=80%:20%; flow rate: 1.0 ml/min. Separation conditions of [.sup.125] 22: Venusil MP C18 reversed phase column (5 m, 4.6250 mm); CH.sub.3CN:10mMAcNH.sub.4=80%:20%; flow rate: 1.0 ml/min. Retention time of .sup.125I labeled ligands and reference compounds is analyzed through HPLC. The obtained .sup.125I labeled ligands are stored at 20 C. for future use.

    [0198] 2) Preparation of Compounds [.sup.18F] 44a, [.sup.18F] 53a and [.sup.18F] 53b

    [0199] See FIG. 2 for the synthesis reaction route. 1.0 mg of each of corresponding labeled precursors (respectively compounds 48, 52a and 52b) is dissolved in 0.8 ml of anhydrous acetonitrile to obtain solution, the solution is added into a dewatered reaction tube containing .sup.l8F.sup. which has certain activity and contains K.sub.222/K.sub.2CO.sub.3, labeling is conducted for 5 min under the condition of 100 C., and 10 ml of deionized water is added after cooling to dilute reaction mixture. Mixed solution is purified through a pretreated Sep-Pak Plus C-18 solid phase extraction small column, then 10 ml of deionized water is used to wash the column to remove unreacted [.sup.18F] F.sup. and inorganic salts, the column is dried by blowing N.sub.2, then 21 ml of anhydrous acetonitrile is used to elute labeled compounds and labeled precursors which are adsorbed onto the column, and separation and purification are conducted through HPLC after concentration, separation conditions: Venusil MP C18 reversed phase column (5 m, 10250 mm); CH.sub.3CN:H.sub.2O=70%:30%; flow rate: 4.0 ml/min. Retention time of .sup.18F labeled ligands and reference compounds is analyzed through HPLC under conditions which are the same as the separation conditions.

    [0200] II. Experiment Results:

    [0201] .sup.125I labeled ligands are prepared through a classic tin-halogen exchange method. Labeling rates of [.sup.125I] 4, [.sup.125I] 24, [.sup.125I] 22, [.sup.125I] 31a and [.sup.125I] 35a are sequentially 86.2%, 94.9%, 92.9%, 67.3% and 27.1%. After separation and purification are conducted through HPLC, radiochemical purity is higher than 95% and the retention time is consistent with the retention time of stable iodo ligands (see Table 1).

    [0202] .sup.18F labeled compounds are prepared through a one-step method. Labelling rates of [.sup.18F] 44a, [.sup.18F] 53a and [.sup.18F] 53b are sequentially 13.8%, 13.4% and 23.9%. After separation and purification are conducted through HPLC, radiochemical purity is higher than 98% and the retention time is consistent with the retention time of stable ligands (see Table 1).

    TABLE-US-00007 TABLE 1 Retention time and purify of .sup.125I and .sup.18F labeled ligands and stable ligands thereof Flow Flow rate phase Chromatographic Retention (mL/ (CH.sub.3CN column (Venusil time Purity Compound min) %) MP C18) (RT, min) (%) 4 1 80 4.6 250 mm 11.43 99.1% [.sup.125I]4 1 80 4.6 250 mm 11.93 98.6% 24 1 80 4.6 250 mm 10.93 99.5% [.sup.1251]24 1 80 4.6 250 mm 11.51 99.0% 22 1 80 4.6 250 mm 12.29 98.5% [.sup.1251]22 1 80 4.6 250 mm 12.86 96.4% 31a I 80 4.6 250 mm 8.81 99.4% [.sup.125I]31a I 80 4.6 250 mm 9.28 99.2% 35a 1 80 4.6 250 mm S.2I 99.7% [.sup.125I]35a 1 80 4.6 250 mm 8.63 98.9% 44a 4 70 10 250 mm 6.64 98.4% [.sup.18F]44a 4 70 10 250 mm 6.77 99.2% 53a 4 70 10 250 mm 9.14 95.4% [.sup.18F]53a 4 70 10 250 mm 9.25 98.4% 53b 4 70 10 250 mm 9.59 96.6% [.sup.18F]53b 4 70 10 250 mm 9.72 98.8%

    Experiment Example 1

    Biological Evaluation

    [0203] In-vitro competitive binding experiments (Ki determination) of compounds 4-25, 31a, 35a, 44a, 46, 47, 53a, 55, 57-59, 65 and 67, IMPY and PIB with A.sub.1-42 aggregates:

    [0204] Binding reaction occurs between A.sub.1-42 aggregate proteins with certain concentration and radioactive ligands [.sup.125I] IMPY, compounds (respectively prepared compounds 4-25, 31a, 35a, 44a, 46, 47, 53a, 55, 57-59, 65 and 67) with different concentration and to be determined, IMPY and PM are simultaneously added into the reaction system to competitively react with [.sup.125I] 4, the compounds are separated after balancing, and the inhibition constant (Ki) is calculated by determining radioactivity.

    [0205] 1. Experiment Steps:

    [0206] (1) Preparing 4 l of PBS (0.2M) buffer solution with pH=7.4;

    [0207] (2) Preparing radioligand [.sup.125] IMPY according to the existing method; preparing the [.sup.125I] IMPY into 100000 cpm/100 L water solution;

    [0208] (3) Preparing the compounds to be determined into 10.sup.3 to 10.sup.9 mol/L continuously diluted ethanol solution;

    [0209] (4) Preparing receptor A.sub.1-42 proteins according to the existing method and diluting the proteins into 30 nM water solution;

    [0210] (5) Soaking a glass fiber filter membrane in PBS solution containing 0.1% (volume fraction) polyethyleneimine for 0.5 h;

    [0211] (6) Respectively adding 100 l of solution of compounds with different concentration and to be determined, 100 l of [.sup.125I] IMPY solution, 700 l of PBS and 100 l of A.sub.1-42 solution in a 1275 mm high borosilicate glass tube; sealing the tube by using a sealing film and whirling;

    [0212] (7) Oscillating and incubating for 2 h in 37 C. constant-temperature water bath;

    [0213] (8) Collecting reaction liquid by using a multi-head cell collector, and washing the reaction liquid for three times by using PBS, 3 ml per time;

    [0214] (9) Measuring and counting by using a counter; and

    [0215] (10) Processing data.

    [0216] 2. Experiment Results

    [0217] See Table 2 for half inhibition constants (IC.sub.50) which are obtained through the competitive binding experiment and the inhibition constants Ki which are further calculated according to a formula.

    ##STR00009##

    TABLE-US-00008 TABLE 2 affinity constants of compounds 4-25, 31a, 35a, 44a, 46, 47, 53a and 53b with A.sub.1-42 aggregates Compound R.sub.1 R.sub.2 X Y.sub.1 Y.sub.2 Ki(nM) 4 p-OMe I O CH CH 28.7 8.0 5 m-OMe I O CH CH 154.5 5.6 6 o-OMe I O CH CH 6107 458 7 p-OH I O CH CH 134.0 28.1 8 m-OH I O CH CH 456.0 135.0 9 o-OH I O CH CH 3348 611 10 PF I O CH CH 126.6 18.2 11 p-Cl I O CH CH 22.3 2.6 12 p-Br I O CH CH 14.1 1.2 13 p-I I O CH CH 25.9 2.4 14 p-H I O CH CH 93.9 6.1 15 p-Bu.sup.t I O CH CH 139.0 20.9 16 p-NH.sub.2 I O CH CH 483.9 53.2 17 m-NH.sub.2 I O CH CH 1815 189 18 o-NH.sub.2 I O CH CH 1216 58 19 p-NHMe I O CH CH 57.0 5.1 20 m-NHMe I O CH CH 701.9 92.4 21 o-NHMe I O CH CH >20000 22 p-NMe.sub.2 I O CH CH 20.9 1.8 23 m-NMe.sub.2 I O CH CH 1057 104 24 I p-OMe O CH CH 58.5 3.5 25 p-OMe I S CH CH 626.9 129.3 31a p-OCH.sub.2CH.sub.2F I O CH CH 24.1 8.8 35a PI OCH.sub.2CH.sub.2F O CH CH 23.0 3.3 44a p-OMe OCH.sub.2CH.sub.2F O CH CH 166.6 34.5 46 p-NHMe OCH.sub.2CH.sub.2F O CH CH 460.4 82.0 47 p-NMe.sub.2 OCH.sub.2CH.sub.2F O CH CH 23.0 5.3 53a POCH.sub.2CH.sub.2F OMe O CH CH 464.9 18.8 55 p-Cl I O N CH 879.8 72.4 57 p-Br I O N CH 163.5 23.0 58 p-I I O CH N .sup.1060 130.0 59 p-I I O N CH 824.0 61.6 65 p-I OCH.sub.2CH.sub.2F O N CH 2079 458 67 p-I NMe.sub.2 NH CH CH 124.4 14.3 1MPY 38.1 2.5 pro 45.9 3.1

    [0218] According to the above-mentioned competitive binding experiments, it can be known that the compounds 4, 11, 12, 13, 22, 31a, 35a and 47 of the compounds described in the present invention have higher affinity with the A.sub.1-42 aggregates, and the affinity of the compounds is higher than that of the known compounds IMPY and PIB.

    [0219] In this experiment example, the structural formulas of the known compounds IMPY and PM are respectively:

    ##STR00010##

    Experiment Example 2

    Autoradiography Experiment

    [0220] After .sup.18F or .sup.125I labeled compounds with certain concentration are respectively bound with plaques in AD transgenic mouse and AD patient brain sections, exposure is conducted through a phosphor screen and then images are analyzed by using a storage phosphor screen system.

    [0221] 1. Experiment Steps:

    [0222] (1) Pretreating the AD transgenic mouse brain section and the AD patient brain section;

    [0223] (2) Respectively covering the AD transgenic mouse brain section or the AD patient brain section with 100 l of 5, Ci .sup.18F or .sup.125I labeled compounds, and incubating for 60 min at room temperature;

    [0224] (3) Sequentially washing the section with lithium carbonate saturated 40% ethanol solution for 5 min and then washing the section with flowing water for 5 min; and

    [0225] (4) After being air-dried, wrapping the section with a preservative film, placing the section under the phosphor screen for exposure for 120 min and analyzing the images by using the storage phosphor screen system.

    [0226] 2. Experiment Results:

    [0227] Experiment results are shown in FIG. 5 and FIG. 6. It fully shows that, after the compounds of the present invention are labeled by radionuclide, the compounds can be used as brain A plaque imaging agents, which can be applied to clinical diagnosis.

    [0228] FIG. 5 shows autoradiography results of [.sup.125I] 4, [.sup.125I] 24 and [.sup.125I] 23 which are respectively applied to human brain sections ((A, E and I) AD, 64-year old, female; (B, F and J) normal, 74-year old, male) and mouse brain sections ((C, G and K) transgenic mice, APPswe/PSEN 1, 11-month old; (D, H and L) normal, C57BL6, 11-month old). Same sections are subjected to dyeing through thioflavin-S for contrast.

    [0229] FIG. 6 shows autoradiography results of [.sup.18F] 53a and [.sup.18F] 53b which are respectively applied to human brain sections ((A and E) AD, 64-year old, female; (B and F) normal, 74-year old, male) and mouse brain sections ((C and G) transgenic mice, APPswe/PSEN 1, 11-month old; (D and H) normal, C57BL6, 11-month old). Same sections are subjected to dyeing through thioflavin-S for contrast.

    Experiment Example 3

    Experiments of Biological Distribution in Bodies of Normal Mice

    [0230] Through in-vivo distribution experiments, pharmacokinetic features, especially initial bran intake and brain removal situations of .sup.18F or .sup.125I labeled compounds in the bodies of mice are studied.

    [0231] 1. Experiment Steps

    [0232] 5-10 Ci labeled compounds (1000 of normal saline solution, containing 5% ethanol) are injected into the bodies of normal mice (ICR, male, 20-22 g, 5-week old) from caudal veins, the mice are beheaded respectively at the moment of 2 min, 10 min, 30 min and 60 min after injection, relevant organs are taken out through dissection, wet weight is measured and radioactive counting is conducted. Data are expressed in radioactive percentage dosage per organ (% ID/organ) and radioactive percentage dosage per gram of organ (% ID/g).

    [0233] 2. Experiment Results

    [0234] Experiment results are shown in Table 3. The .sup.18F or .sup.125I labeled compounds of the present invention can smoothly pass through blood brain barriers, brain intake reaches a peak at the moment of 2 min, the removing speed in the brains of normal mice is very fast and the ratio of brain intake at the moment of 2 min to brain intake at the moment of 60 min reaches approximate 10. Through further comparison with the known compounds such as [.sup.125I] IMPY in the prior art, it can be found that the removing speed of the phenyl benzyl ether compounds in the brains of the normal mice is obviously superior to that of the known compounds.

    [0235] In this experiment example, the structural formula of the known compound [.sup.125I] IMPY is:

    ##STR00011##

    TABLE-US-00009 TABLE 3 distribution results .sup.a of [.sup.125I] 4, [.sup.125I] 24, [.sup.125I] 22, [.sup.125I] 31a, [.sup.125I] 35a, [.sup.125I] IMPY, [.sup.18F] 44a, [.sup.18F] 53a and [.sup.18F] 53b in bodies of normal mice Organ 2 min 10 min 30 min 60 min [.sup.125I]4 (logD = 4.00 0.08) Blood 3.03 0.54 3.32 0.65 2.56 0.93 1.70 0.50 Brain 6.18 0.99 3.54 0.35 0.88 0.15 0.38 0.05 Thyroid.sup.b 0.14 0.04 0.12 0.04 0.08 0.01 0.11 0.02 [.sup.125I]24 (logD = 4.16 0.29) Blood 5.13 0.62 4.26 0.38 3.31 0.79 2.60 1.33 Brain 4.29 1.06 2.11 0.38 0.73 0.17 0.32 0.09 Thyroid.sup.b 0.07 ( ).( )1 0.07 0.03 0.17 0.03 0.19 0.05 [.sup.125I]22 (logD = 2.89 0.09) Blood 4.01 0.28 2.46 0.30 2.53 0.27 1.34 0.26 Brain 4.91 0.60 3.26 0.24 1.34 0.12 0.49 0.07 Thyroid.sup.b 0.11 0.03 0.12 0.03 0.16 0.04 0.27 0.04 [.sup.125I]31a (logD = 3.96 0.22) Blood 5.03 0.20 3.03 0.48 2.17 0.31 1.% 0.31 Brain 7.04 0.89 2.73 0.25 1.05 0.22 0.55 0.11 Thyroid.sup.b 0.12 0.02 0.09 + 0.02 0.12 0.01 0.16 0.03 [.sup.125I]35a (logD = 2.50 0.23) Blood 4.96 0.35 3.88 0.79 3.89 0.53 3.01 1.07 Brain 5.27 0.98 2.28 0.27 0.81 + 0.06 0.37 0.06 Thyroid.sup.b 0.13 0.02 0.13 0.01 0.19 0.04 0.34 0.10 [.sup.125I]IMPY Blood 3.85 0.53 2.81 0.33 1.50 0.20 1.03 0.10 Brain 5.05 0.38 1.80 0.12 0.67 0.15 0.45 0.07 Thyroid.sup.b 0.12 0.05 0.09 0.03 0.22 0.08 0.30 0.09 [.sup.18F]44a (logD = 3.05 0.08) Blood 3.90 0.25 3.86 0.24 4.28 0.23 3.86 0.39 Brain 7.54 0.39 3.32 0.38 2.77 0.22 2.33 0.30 Bone.sup.b 1.50 0.44 1.04 0.25 1.43 0.44 4.05 0.62 [.sup.18F] 53a (logD = 3.65 0.04) Blood 4.26 0.41 4.61 0.95 3.76 0.19 3.05 1.09 Brain 9.95 2.36 2.77 + 0.19 1.44 0.18 1.30 0.16 Bone.sup.b 2.37 0.69 2.76 0.47 4.02 0.78 5.89 0.49 [.sup.18F] 53b (logD = 3.04 0.04) Blood 3.95 0.34 4.14 0.91 3.40 0.25 2.36 0.66 Brain 9.71 1.31 2.52 0.20 1.39 0.10 1.07 0.10 Bone.sup.b 1.36 0.35 1.22 0.42 1.39 0.54 1.52 0.27 .sup.ais expressed in % ID/g, n = 4-5. .sup.bis expressed in % ID/organ.

    [0236] Although the present invention has been described above in details by using general description and specific embodiments, some modifications or improvements can be made on the basis of the present invention and it is obvious for one skilled in the art. Therefore, any modifications or improvements made without departing from the spirit of the present invention belong to the protection scope claimed by the present invention.