SYNTHETIC METHODS OF PREPARING ESKETAMINE

Abstract

The present invention is directed to methods for the asymmetric synthesis of esketamine. The present invention is further directed to key intermediates in the asymmetric esketamine synthesis. In one embodiment, the invention is an asymmetric synthesis of esketamine comprising the conversion of (S)-2′-chloro-2-methoxy-3,4,5,6-5 tetrahydro-[1,1′-biphenyl]-3-yl carbamate to (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl.

##STR00001##

Claims

1. An asymmetric synthesis of esketamine, D3-esketamine, or (S)-norketamine comprising conversion of (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate to (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl ##STR00072##

2. The asymmetric esketamine synthesis of claim 1, further comprising reduction of (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl to form (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine ##STR00073## wherein said reduction is characterized by the use of lithium aluminum hydride.

3. The asymmetric synthesis of claim 2, further comprising deprotection of (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine to form esketamine ##STR00074## wherein said deprotection is characterized by the use of hydrochloric acid.

4. The asymmetric synthesis of claim 3, wherein the (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate is prepared by asymmetric reduction of 2′-chloro-2-methoxy-5,6-dihydro-[1,1′-biphenyl]-3(4H)-one: ##STR00075## wherein said reduction is characterized by the use of (S,S)-Teth-TsDpen RuCl, followed by the use of trichloroacetyl isocyanate.

5. The asymmetric synthesis of claim 3, wherein the (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate is prepared by asymmetric reduction of 2′-chloro-2-methoxy-5,6-dihydro-[1,1′-biphenyl]-3(4H)-one: ##STR00076## wherein said reduction is characterized by the use of (S,S)-Teth-TsDpen RuCl, followed by the use of trichloroacetyl isocyanate.

6. The asymmetric D3-esketamine synthesis of claim 1, wherein the asymmetric synthesis of D3-esketamine further comprises the steps described below: reduction of (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl to form (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine ##STR00077## wherein said reduction is characterized by the use of lithium aluminum deuteride, and deprotection of (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine to form D3-esketamine ##STR00078## wherein said deprotection is characterized by the use of hydrochloric acid.

7. The asymmetric (S)-norketamine synthesis of claim 1, wherein the asymmetric synthesis of (S)-norketamine further comprises conversion of (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl to (S)-norketamine ##STR00079## wherein said conversion is characterized by the use of hydrochloric acid.

8. A compound which is (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate ##STR00080##

9. A compound which is (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl ##STR00081##

Description

[0018] ##STR00003##

DETAILED DESCRIPTION OF THE INVENTION

[0019] The present invention is directed to methods for the asymmetric synthesis of esketamine.

[0020] In one embodiment, the invention is an asymmetric synthesis of esketamine, D3-esketamine, or (S)-norketamine comprising the conversion of (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate to (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl

##STR00004##

[0021] In another embodiment, the invention is an asymmetric synthesis of esketamine comprising the steps described below:

a) conversion of (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate to (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl

##STR00005##

and
b) reduction of (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl to form (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine

##STR00006##

wherein said reduction is characterized by the use of lithium aluminum hydride.

[0022] In another embodiment, the invention is an asymmetric synthesis of esketamine comprising the steps described below:

a) conversion of (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate to (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl

##STR00007##

b) reduction of (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl to form (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine

##STR00008##

wherein said reduction is characterized by the use of lithium aluminum hydride, and
c) deprotection of (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine to form esketamine

##STR00009##

wherein said deprotection is characterized by the use of hydrochloric acid.

[0023] In another embodiment, the invention is an asymmetric synthesis of esketamine comprising the steps described below:

a) conversion of (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate to (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl

##STR00010##

b) reduction of (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl to form (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine

##STR00011##

wherein said reduction is characterized by the use of lithium aluminum hydride,
c) deprotection of (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine to form esketamine

##STR00012##

wherein said deprotection is characterized by the use of hydrochloric acid, and
d) wherein the (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate used in step a) is prepared by asymmetric reduction of 2′-chloro-2-methoxy-5,6-dihydro-[1,1′-biphenyl]-3(4H)-one:

##STR00013##

wherein said reduction is characterized by the use of (S,S)-Teth-TsDpen RuCl, followed by the use of trichloroacetyl isocyanate.

[0024] In another embodiment, the invention is an asymmetric synthesis of D3-esketamine comprising the steps described below:

a) conversion of (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate to (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl

##STR00014##

b) reduction of (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl to form (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine

##STR00015##

wherein said reduction is characterized by the use of lithium aluminum deuteride, and
c) deprotection of (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine to form D3-esketamine

##STR00016##

wherein said deprotection is characterized by the use of hydrochloric acid.

[0025] In another embodiment, the invention is an asymmetric synthesis of (S)-norketamine comprising the steps described below:

a) conversion of (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate to (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl

##STR00017##

b) conversion of (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl to (S)-norketamine

##STR00018##

wherein said conversion is characterized by the use of hydrochloric acid.

[0026] Another embodiment of the invention is a compound which is (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate

##STR00019##

[0027] Another embodiment of the invention is a compound which is (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl

##STR00020##

[0028] In one embodiment, the invention is an asymmetric synthesis of esketamine, D3-esketamine, or (S)-norketamine comprising the conversion of (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate to (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl

##STR00021##

wherein said conversion is characterized by the use of trifluoroacetic anhydride and triethylamine.

[0029] In another embodiment, the invention is an asymmetric synthesis of esketamine comprising the steps described below:

a) conversion of (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate to (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl

##STR00022##

wherein said conversion is characterized by the use of trifluoroacetic anhydride and triethylamine, and
b) reduction of (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl to form (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine

##STR00023##

wherein said reduction is characterized by the use of lithium aluminum hydride.

[0030] In another embodiment, the invention is an asymmetric synthesis of esketamine comprising the steps described below:

a) conversion of (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate to (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl

##STR00024##

wherein said conversion is characterized by the use of trifluoroacetic anhydride and triethylamine,
b) reduction of (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl to form (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine

##STR00025##

wherein said reduction is characterized by the use of lithium aluminum hydride, and
c) deprotection of (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine to form esketamine

##STR00026##

wherein said deprotection is characterized by the use of hydrochloric acid.

[0031] In another embodiment, the invention is an asymmetric synthesis of esketamine comprising the steps described below:

a) conversion of (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate to (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl

##STR00027##

wherein said conversion is characterized by the use of trifluoroacetic anhydride and triethylamine,
b) reduction of (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl to form (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine

##STR00028##

wherein said reduction is characterized by the use of lithium aluminum hydride,
c) deprotection of (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine to form esketamine

##STR00029##

wherein said deprotection is characterized by the use of hydrochloric acid, and
d) wherein the (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate used in step a) is prepared by asymmetric reduction of 2′-chloro-2-methoxy-5,6-dihydro-[1,1′-biphenyl]-3(4H)-one:

##STR00030##

wherein said reduction is characterized by the use of (S,S)-Teth-TsDpen RuCl, followed by the use of trichloroacetyl isocyanate.

[0032] In another embodiment, the invention is an asymmetric synthesis of esketamine comprising the steps described below: [0033] a) conversion of (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate to (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl

##STR00031##

wherein said conversion is characterized by the use of trifluoroacetic anhydride and triethylamine,
b) reduction of (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl to form (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine

##STR00032##

wherein said reduction is characterized by the use of lithium aluminum hydride,
c) deprotection of (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine to form esketamine

##STR00033##

wherein said deprotection is characterized by the use of hydrochloric acid, and
d) wherein the (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate used in step a) is prepared by asymmetric reduction of 2′-chloro-2-methoxy-5,6-dihydro-[1,1′-biphenyl]-3(4H)-one:

##STR00034##

wherein said reduction is characterized by the use of (S,S)-Teth-TsDpen RuCl, followed by the use of trichloroacetyl isocyanate.

[0034] In another embodiment, the invention is an asymmetric synthesis of D3-esketamine comprising the steps described below:

a) conversion of (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate to (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl

##STR00035##

wherein said conversion is characterized by the use of trifluoroacetic anhydride and triethylamine,
b) reduction of (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl to form (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine

##STR00036##

wherein said reduction is characterized by the use of lithium aluminum deuteride, and
c) deprotection of (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine to form D3-esketamine

##STR00037##

wherein said deprotection is characterized by the use of hydrochloric acid.

[0035] In another embodiment, the invention is an asymmetric synthesis of (S)-norketamine comprising the steps described below:

a) conversion of (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate to (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl

##STR00038##

wherein said conversion is characterized by the use of trifluoroacetic anhydride and triethylamine,
b) conversion of (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl to (S)-norketamine

##STR00039##

wherein said conversion is characterized by the use of hydrochloric acid.

[0036] The invention may be more fully appreciated by reference to the following description, including the following glossary of terms and the concluding examples.

[0037] As used herein, the terms “including”, “containing” and “comprising” are used herein in their open, non-limiting sense.

Definitions

[0038] As used herein, the term “esketamine” shall mean the (S)-enantiomer of ketamine,

##STR00040##

also known as (S)-2-(2-chlorophenyl)-2-(methylamino)cyclohexanone.

[0039] As used herein, the term “D3-esketamine” shall mean the (S)-enantiomer of D3-ketamine,

##STR00041##

also known as (S)-2-(2-chlorophenyl)-2-((methyl-d3)amino)cyclohexan-1-one.

[0040] As used herein, the term “(S)-norketamine” shall mean the (S)-enantiomer of norketamine,

##STR00042##

Also known as (S)-2-amino-2-(2-chlorophenyl)cyclohexan-1-one.

[0041] As used herein, the term “asymmetric synthesis”, is a form of chemical synthesis wherein one enantiomer is formed in excess over another enantiomer.

[0042] As used herein, the term “(S,S)-Teth-TsDpen RuCl”, is chloro[(S,S)-1,2-diphenyl-N1-(3-phenylpropyl)-N2-(p-toluenesulfonyl)-1,2-ethanediamine]ruthenium(II), for further clarity, (S,S)-Teth-TsDpen RuCl is

##STR00043##

[0043] Where the compounds according to this invention have at least one stereocenter, they may exist as enantiomers. It is to be understood that all such enantiomers and mixtures thereof are encompassed within the scope of the present invention.

[0044] Where the reactions according to this invention give rise to an excess of at least one stereocenter, said reactions may be characterized as generating an enantiomeric excess of the resulting stereocenter in the product. It is to be understood that all such enantiomeric excesses are encompassed within the scope of the present invention. For example, an enantiomeric excess of at least 80% is considered to be within the scope of the invention. For additional example, an enantiomeric excess of at least 90% is considered to be within the scope of the invention. For additional example, an enantiomeric excess of at least 95% is considered to be within the scope of the invention. For additional example, an enantiomeric excess of at least 97% is considered to be within the scope of the invention.

[0045] Additionally, any formula given herein is intended to refer also to hydrates, solvates, and polymorphs of such compounds, and mixtures thereof, even if such forms are not listed explicitly.

[0046] Any formula given herein is also intended to represent unlabeled forms as well as isotopically labeled forms of the compounds. Isotopically labeled compounds have structures depicted by the formulas given herein except that one or more atoms are replaced by an atom having a selected atomic mass or mass number. Examples of isotopes that can be incorporated into compounds of the invention include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorus, fluorine, and chlorine, such as .sup.2H, .sup.3H, .sup.11C, .sup.13C, .sup.14C, .sup.15N, .sup.18O, .sup.17O, respectively. Such isotopically labeled compounds are useful in metabolic studies (preferably with .sup.14C), reaction kinetic studies (with, for example .sup.2H or .sup.3H), detection or imaging techniques [such as positron emission tomography (PET) or single-photon emission computed tomography (SPECT)] including drug or substrate tissue distribution assays, or in radioactive treatment of patients. Further, substitution with heavier isotopes such as deuterium (i.e., .sup.2H or D) may afford certain therapeutic advantages resulting from greater metabolic stability, for example increased in vivo half-life or reduced dosage requirements. Isotopically labeled compounds of this invention and prodrugs thereof can generally be prepared by carrying out the procedures disclosed in the schemes or in the examples and preparations described below by substituting a readily available isotopically labeled reagent for a non-isotopically labeled reagent.

[0047] Those skilled in the art will recognize that compounds and reagents used in the reactions of the invention may exist as salts. The invention contemplates the use of all salts of any compound used in a reaction exemplified herein.

[0048] Examples of salts include, without limitation, sulfates, pyrosulfates, bisulfates, sulfites, bisulfites, phosphates, monohydrogen-phosphates, dihydrogenphosphates, metaphosphates, pyrophosphates, chlorides, bromides, iodides, acetates, propionates, decanoates, caprylates, acrylates, formates, isobutyrates, caproates, heptanoates, propiolates, oxalates, malonates, succinates, suberates, sebacates, fumarates, maleates, butyne-1,4-dioates, hexyne-1,6-dioates, benzoates, chlorobenzoates, methylbenzoates, dinitrobenzoates, hydroxybenzoates, methoxybenzoates, phthalates, sulfonates, xylenesulfonates, phenylacetates, phenylpropionates, phenylbutyrates, citrates, lactates, γ-hydroxybutyrates, glycolates, tartrates, methane-sulfonates, propanesulfonates, naphthalene-1-sulfonates, naphthalene-2-sulfonates, and mandelates. In some embodiments, the compound is the hydrochloride salt of esketamine.

[0049] When a compound or reagent used in a reaction of the invention contains a basic nitrogen, a salt may be prepared by any suitable method available in the art, for example, treatment of the free base with an inorganic acid, such as hydrochloric acid, hydrobromic acid, sulfuric acid, sulfamic acid, nitric acid, boric acid, phosphoric acid, and the like, or with an organic acid, such as acetic acid, phenylacetic acid, propionic acid, stearic acid, lactic acid, ascorbic acid, maleic acid, hydroxymaleic acid, isethionic acid, succinic acid, valeric acid, fumaric acid, malonic acid, pyruvic acid, oxalic acid, glycolic acid, salicylic acid, oleic acid, palmitic acid, lauric acid, a pyranosidyl acid, such as glucuronic acid or galacturonic acid, an alpha-hydroxy acid, such as mandelic acid, citric acid, or tartaric acid, an amino acid, such as aspartic acid, glutaric acid or glutamic acid, an aromatic acid, such as benzoic acid, 2-acetoxybenzoic acid, naphthoic acid, or cinnamic acid, a sulfonic acid, such as laurylsulfonic acid, p-toluenesulfonic acid, methanesulfonic acid, ethanesulfonic acid, any compatible mixture of acids such as those given as examples herein, and any other acid and mixture thereof that are regarded as equivalents or acceptable substitutes in light of the ordinary level of skill in this technology.

[0050] Exemplary reactions useful in methods of the invention will now be described by reference to the illustrative synthetic schemes for their general preparation below and the specific examples that follow. Those skilled in the art will recognize that reactions may be performed in any suitable solvent. Those skilled in the art will also recognize that, except where specifically limited, reactions may be performed at a wide range of temperatures. Unless otherwise specified, reactions may be performed between the melting point and the reflux temperature of the solvent, and preferably between 0° C. and the reflux temperature of the solvent. Reactions may be heated employing conventional heating or microwave heating. Reactions may also be conducted in sealed pressure vessels above the normal reflux temperature of the solvent.

Abbreviations

[0051] Herein and throughout the specification, the flowing abbreviations may be used.

TABLE-US-00001 Abbreviation Term DCM dichloromethane DIPEA diisopropyl ethylamine EtOAc ethyl acetate EtOH ethanol Et.sub.3N triethylamine h hours HOAc acetic acid HPLC high-performance liquid chromatography MeOH methanol OAc acetate PPh.sub.3 triphenylphosphine TBAF tetrabutylammonium fluoride TFAA trifluoroacetic acid anhydride Tf.sub.2O trifluoromethane sulfonic anhydride THF tetrahydrofuran TLC thin layer chromatography (S,S)-Teth-TsDpen chloro[(S,S)-1,2-diphenyl-N1-(3- RuCl phenylpropy1)-N2- (p-toluenesulfony1)-1,2- ethanediamine]ruthenium(II)

Numbered Embodiments

[0052] 1. An asymmetric synthesis of esketamine, D3-esketamine, or (S)-norketamine comprising

[0053] conversion of (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate to (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl

##STR00044##

2. The asymmetric esketamine synthesis of numbered embodiment 1, further comprising reduction of (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl to form (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine

##STR00045##

3. The asymmetric esketamine synthesis of numbered embodiment 1 or 2, further comprising reduction of (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl to form (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine

##STR00046##

wherein said reduction is characterized by the use of lithium aluminum hydride.
4. The asymmetric synthesis of numbered embodiment 2 or 3, further comprising deprotection of (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine to form esketamine

##STR00047##

5. The asymmetric synthesis of any one of numbered embodiments 2-4, further comprising deprotection of (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine to form esketamine

##STR00048##

wherein said deprotection is characterized by the use of hydrochloric acid.
6. The asymmetric synthesis of any one of numbered embodiments 1-5, wherein the (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate is prepared by asymmetric reduction of 2′-chloro-2-methoxy-5,6-dihydro-[1,1′-biphenyl]-3(4H)-one:

##STR00049##

7. The asymmetric synthesis of any one of numbered embodiments 1-6, wherein the (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate is prepared by asymmetric reduction of 2′-chloro-2-methoxy-5,6-dihydro-[1,1′-biphenyl]-3(4H)-one, followed by the use of trichloroacetyl isocyanate:

##STR00050##

8. The asymmetric synthesis of any one of numbered embodiments 1-7, wherein the (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate is prepared by asymmetric reduction of 2′-chloro-2-methoxy-5,6-dihydro-[1,1′-biphenyl]-3(4H)-one:

##STR00051##

wherein said reduction is characterized by the use of (S,S)-Teth-TsDpen RuCl, followed by the use of trichloroacetyl isocyanate.
9. The asymmetric synthesis of any one of numbered embodiments 1-7, wherein the (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate is prepared by asymmetric reduction of 2′-chloro-2-methoxy-5,6-dihydro-[1,1′-biphenyl]-3(4H)-one:

##STR00052##

wherein said reduction is characterized by the use of (S,S)-Teth-TsDpen RuCl, followed by the use of trichloroacetyl isocyanate.
10. The asymmetric D3-esketamine synthesis of numbered embodiment 1, wherein the asymmetric synthesis of D3-esketamine further comprises the steps described below:
reduction of (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl to form (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine

##STR00053##

and deprotection of (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine to form D3-esketamine

##STR00054##

11. The asymmetric D3-esketamine synthesis of numbered embodiment 1 or 10, wherein the asymmetric synthesis of D3-esketamine further comprises the steps described below:
reduction of (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl to form (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine

##STR00055##

wherein said reduction is characterized by the use of lithium aluminum deuteride, and
deprotection of (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine to form D3-esketamine

##STR00056##

wherein said deprotection is characterized by the use of hydrochloric acid.
12. The asymmetric (S)-norketamine synthesis of numbered embodiment 1, wherein the asymmetric synthesis of (S)-norketamine further comprises conversion of (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl to (S)-norketamine

##STR00057##

13. The asymmetric (S)-norketamine synthesis of numbered embodiment 1 or 12, wherein the asymmetric synthesis of (S)-norketamine further comprises conversion of (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl to (S)-norketamine

##STR00058##

wherein said conversion is characterized by the use of hydrochloric acid.
14. A compound which is (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate

##STR00059##

15. A compound which is (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl

##STR00060##

General Scheme

[0054] ##STR00061##

[0055] Scheme 1 shows the asymmetric synthesis of esketamine.

[0056] Achiral ketone 2 may be reduced to chiral alcohol 3 using a reductant, such as formic acid, and a chiral catalyst, for example (S,S)-Teth-TsDpen RuCl. Those skilled in the art will recognize that (RR)-Teth-TsDpen RuCl may be used for the asymmetric synthesis of (R)-ketamine, D3-(R)-ketamine, or (R)-norketamine. Furthermore, those skilled in the art will recognize that asymmetric reduction of a ketone to a chiral alcohol may be accomplished by a number of reductants and a number of chiral catalysts, some of which are described by Masahiro Yoshimura, Shinji Tanaka, and Masato Kitamura in Recent topics in catalytic asymmetric hydrogenation of ketones; Tet. Lett. 55, 2014, 3635-3640 and references cited therein.

[0057] Alcohol 3 may be converted to carbamate 4 using trichloroacetyl isocyanate in a suitable solvent, such as but not limited to DCM.

[0058] Carbamate 4 rearrangement to isocyanate 5 may be performed under a variety of conditions, typically involving a dehydrating agent, a base, and low temperature. For example and without limitation, a carbamate to isocyanate rearrangement may be performed using TFAA and Et.sub.3N at 0° C., as described in example 3 below. Alternatively, the carbamate to isocyanate rearrangement may be performed using Tf.sub.2O and DIPEA at −78° C. Alternatively, the carbamate to isocyanate rearrangement may be performed using PPh.sub.3 and CBr.sub.4 with Et.sub.3N at −20° C. Many other combinations will be known to those skilled in the art, and the invention contemplates the use of all common means of carbamate-isocyanate rearrangement, including those described in Eur. J. Org. Chem. 2017, 1295-1307.

[0059] Conversion of isocyanate 5 to ketamine may be accomplished with a reductant, such as LiAlH.sub.4, followed by deprotection with an acid such as HCl.

##STR00062##

[0060] Scheme 2 shows the conversion of isocyanate 5 to D3-esketamine.

[0061] Conversion of isocyanate 5 to D3-ketamine may be accomplished with a deuterated reductant, such as LiAlD.sub.4, followed by deprotection with an acid such as HCl.

##STR00063##

[0062] Scheme 3 shows the conversion of isocyanate 5 to (S)-norketamine.

[0063] Conversion of isocyanate 5 to norketamine may be accomplished with an acid such as HCl.

[0064] The following examples are for illustrative purposes only and are in no way meant to be limitation of the invention.

EXAMPLES

[0065] In obtaining the compounds described in the examples below and the corresponding analytical data, the following experimental and analytical protocols were followed unless otherwise indicated.

[0066] Unless otherwise stated, reaction mixtures were stirred at room temperature (rt) under a nitrogen atmosphere. Where mixtures, solutions, and extracts were “concentrated”, they were typically concentrated under reduced pressure.

[0067] Normal-phase column chromatography was carried out with Sunasiachem silica gel (300-400 mesh), eluting with the indicated solvents.

[0068] High resolution mass spectra were recorded on Agilent 6030 TOF LC/MS machine using ESI (electrospray ionization). Calculated (calcd.) mass corresponds to the exact mass.

[0069] The optical rotation data were recorded on Autopol I-AP-S2 polarimeter. The melting point data were recorded on WRS-2A Micro Processor Melting-point Apparatus (uncalibrated).

[0070] .sup.1H NMR and .sup.13C NMR spectra were recorded on a Varian 400 NMR Spectrometer with chemical shifts reported in ppm relative to Me.sub.4Si for .sup.1H NMR and CDCl.sub.3 or DMSO-d.sup.6 for .sup.13C NMR, (multiplicity, coupling constant J in Hz, integration).

[0071] Chemical names were generated using ChemDraw Ultra 6.0.2 (CambridgeSoft Corp., Cambridge, Mass.) or ACD/Name Version 9 (Advanced Chemistry Development, Toronto, Ontario, Canada).

[0072] All commercially available reagents were used as received.

Intermediates

Synthesis of 2′-chloro-2-methoxy-5,6-dihydro-[1,1′-biphenyl]-3(4H)-one

[0073] ##STR00064##

[0074] To a solution of crude 3-bromo-2-methoxycyclohex-2-en-1-one (prepared according to the procedure described in Harmata, M.; Bohnert, G.; Kurti, L.; Barnes, C. L. Tetrahedron Lett. 2002, 43, 2347) (1.31 g, 6.39 mmol, 1.0 eq.) in THF (20 mL) was added 2-chlorophenyl boric acid (1.30 g, 8.31 mmol, 1.3 eq.), Pd(OAc).sub.2 (72 mg, 0.319 mmol, 5 mol %), PPh.sub.3 (168 mg, 0.639 mmol, 0.1 eq.) and a solution of K.sub.2CO.sub.3 (3.53 g, 25.6 mmol, 4 eq.) in H.sub.2O (12 mL) under N2 atmosphere. The biphasic mixture was stirred at 50° C. for 1 h, or until the bromo enone was consumed by TLC. The mixture was cooled to room temperature and diluted with EtOAc. The reaction was partitioned and extracted with EtOAc once. The combined organic layers were dried over Na.sub.2SO.sub.4, concentrated, and purified by silica gel column chromatography (eluted with EtOAc/heptane 1/5) to give the titled compound as a light yellow oil (853 mg, 88% yield). .sup.1H NMR (400 MHz, CDCl.sub.3) δ 7.39-7.32 (m, 1H), 7.24-7.16 (m, 2H), 7.14-7.07 (m, 1H), 3.42 (s, 3H), 2.56 (br s, 2H), 2.53 (t, J=6.7 Hz, 2H), 2.08-2.01 (m, 2H). .sup.13C NMR (100 MHz, CDCl.sub.3) δ 195.5, 149.2, 143.4, 137.1, 131.5, 129.7, 129.1, 129.3, 126.8, 59.9, 39.0, 31.0, 22.6. HRMS (ESI) calcd. for C.sub.13H.sub.14ClO.sub.2 [M+H].sup.+: 237.0682, found: 237.0677.

Example 1

Synthesis of (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-ol

[0075] ##STR00065##

[0076] A solution of bromo enone 2 (3.0 g, 12.7 mmol, 1.0 eq.), (S,S)-Teth-TsDpen RuCl (7.9 mg, 0.013 mmol, 0.1 mol %) and HCO.sub.2H/Et.sub.3N (2/3, v/v, 30 mL) was bubbled with N2 at room temperature for 1 h. The mixture was heated to 80° C. and stirred for 2 h or until the enone was consumed by TLC. The reaction was cooled to room temperature and diluted with EtOAc and water. The organic layer was washed with HCl (3 N aq.) three times, and then washed with brine. The organic layer was dried with Na.sub.2SO.sub.4, concentrated, and purified by silica gel column chromatography (eluted with EtOAc/heptane 1/5) to give the alcohol 3 as a light yellow oil (2.8 g, 93% yield). [α].sub.D.sup.20=−89.2 (c 2.5, EtOH). .sup.1H NMR (400 MHz, CDCl.sub.3) δ 7.38-7.36 (m, 2H), 7.25-7.16 (m, 3H), 4.42 (s, 1H), 3.39 (s, 3H), 2.26-2.17 (br m, 3H), 1.93 (br s, 2H), 1.84-1.79 (m, 1H), 1.71-1.66 (m, 1H). .sup.13C NMR (100 MHz, CDCl.sub.3) δ 151.3, 139.1, 133.0, 130.6, 129.4, 128.1, 126.6, 119.6, 64.8, 57.7, 31.7, 30.4, 18.5. HRMS (ESI) calcd. for C.sub.13H.sub.16ClO.sub.2 [M+H].sup.+: 239.0839, found: 239.0833.

Example 2a

Synthesis of (S)-2′-chloro-2-methoxy-3,4,5,6-tetrahydro-[1,1′-biphenyl]-3-yl carbamate

[0077] ##STR00066##

[0078] To a solution of 3 (1.5 g, 6.28 mmol, 1.0 eq.) in DCM (42 mL) at 0° C. was added trichloroacetyl isocyanate (2.37 g, 12.6 mmol, 2.0 eq.). The reaction solution was stirred at 0° C. for 15 min, warmed to room temperature, and stirred for an additional 15 min. After the allylic alcohol was consumed by TLC, the reaction solution was concentrated to dryness and diluted with MeOH (45 mL). The reaction was diluted with a solution of K.sub.2CO.sub.3 (6.95 g, 50.3 mmol, 8.0 eq.) in H.sub.2O (25 mL), stirred for 2 h, concentrated, and diluted with EtOAc and water. The reaction was partitioned and the aqueous layer was extracted with EtOAc twice. The combined organic layers were dried over MgSO.sub.4, concentrated, and purified by silica gel column chromatography (eluted with MeOH/DCM 1/100) to obtain the carbamate 4 as a white solid (1.79 g, 100% yield). [α].sub.D.sup.20=−91.2 (c 2.5, EtOH). M.P. 181° C. .sup.1H NMR (400 MHz, CDCl.sub.3) δ 7.39-7.37 (m, 1H), 7.23-7.18 (m, 3H), 5.51 (s, 1H), 4.67 (s, 2H), 3.37 (s, 3H), 2.29 (br s, 2H), 2.10-2.04 (m, 1H), 1.92-1.85 (m, 1H), 1.82-1.68 (m, 2H). .sup.13C NMR (100 MHz, DMSO-d.sup.6) S 156.7, 148.3, 139.3, 132.4, 131.1, 129.6, 128.9, 127.5, 64.9, 56.4, 30.0, 18.2. HRMS (ESI) calcd. for C.sub.14H.sub.17ClNO.sub.3 [M+H].sup.+: 282.0897, found: 282.0891.

Example 2b

Alternative Prophetic Method

[0079] A suspension of NaOCN (2.72 g, 41.9 mmol, 2.0 eq.) in DCM (15 mL) is added a solution of 3 (5 g, 21.0 mmol, 1.0 eq.) in DCM (5 mL) at 0° C., followed by TFA (5.02 g, 44.0 mmol, 2.1 eq.). The reaction solution is stirred at 0° C. for 15 min, warmed to room temperature, and stirred for 12 h. After the allylic alcohol is consumed by TLC, the reaction is quenched with H.sub.2O (50 mL), partitioned, and the organic layer is extracted with DCM (50 mL) three times. The combined organics are dried over MgSO.sub.4, concentrated, and purified on silica gel by column chromatography (eluted with MeOH/DCM 1/100), to give the carbamate 4.

Example 3

Synthesis of (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl

[0080] ##STR00067##

[0081] To a stirred solution of carbamate 4 (800 mg, 2.84 mmol, 1.0 eq.) and Et.sub.3N (1.2 mL, 8.52 mmol, 3.0 eq.) in DCM (8 mL) at 0° C. was added TFAA (0.60 mL, 4.26 mmol, 1.5 eq.). After 2 h, the carbamate was consumed by TLC, quenched with H.sub.2O, and diluted with DCM. The organic layer was dried over MgSO.sub.4, concentrated under vacuum, and purified by column chromatography using basic silica gel (eluted with EtOAc/heptane 1/50) to obtain isocyanate 5 as a yellow oil (654 mg, 88% yield). [α].sub.D.sup.20=+7.1 (c 1.7, EtOH). .sup.1H NMR (400 MHz, CDCl.sub.3) δ 7.70 (dd, J=7.8, 1.6 Hz, 1H), 7.34 (dd, J=7.7, 1.5 Hz, 1H), 7.24 (dtd, J=24.0, 7.5, 1.6 Hz, 2H), 4.93 (t, J=4.2 Hz, 1H), 3.54 (s, 3H), 2.43 (ddd, J=13.6, 12.2, 3.3 Hz, 1H), 2.29-2.25 (m, 2H), 1.90 (ddd, J=13.5, 5.1, 2.9 Hz, 1H), 1.85-1.75 (m, 1H), 1.74-1.64 (m, 1H). .sup.13C NMR (100 MHz, CDCl.sub.3) δ 154.3, 139.9, 131.3, 131.2, 129.4, 129.3, 128.6, 126.7, 97.5, 65.7, 54.7, 37.6, 23.3, 19.4. HRMS (ESI) calcd. for C.sub.14H.sub.15ClNO.sub.2 [M+H].sup.+: 264.0791, found: 264.0786.

Example 4

Synthesis of (S)-2′-chloro-6-methoxy-N-methyl-3,4-dihydro-[1,1′-biphenyl]-1(2H)-amine

[0082] ##STR00068##

[0083] To a slurry of excess LiAlH.sub.4 (115 mg, 3.03 mmol, 2.0 eq.) in THF (5 mL) was added a solution of isocyanate 5 (400 mg, 1.52 mmol, 1.0 eq.) in THF (5 mL). The reaction was heated to 70° C., stirred for 3 h, cooled to room temperature and quenched with a 30% NaOH aqueous solution (20 mL). The reaction was then heated to 90° C., stirred for 30 min, cooled to room temperature, and diluted with DCM. The reaction was partitioned and the aqueous layer was extracted with DCM once. The combined organic layers were dried over MgSO.sub.4, concentrated, and purified with by silica gel column chromatography (eluted with EtOAc/heptane 1/3) to obtain methyl amine 6 as a light yellow oil (308 mg, 80% yield). [α].sub.D.sup.20=−80.5 (c 2.1, EtOH). .sup.1H NMR (400 MHz, CDCl.sub.3) δ 7.46 (dt, J=7.7, 1.7 Hz, 1H), 7.31 (dt, J=7.8, 1.5 Hz, 1H), 7.23-7.10 (m, 2H), 4.90 (t, J=3.9 Hz, 1H), 3.52 (s, 3H), 2.43-2.37 (m, 1H), 2.35 (s, 3H), 2.19-2.16 (m, 2H), 1.83-1.76 (m, 1H), 1.66-1.57 (m, 1H), 1.42-1.30 (m, 1H). .sup.13C NMR (100 MHz, CDCl.sub.3) δ 156.1, 141.2, 132.8, 131.53, 131.47, 127.8, 126.2, 97.5, 63.5, 53.8, 34.0, 31.4, 23.9, 19.3. HRMS (ESI) calcd. for C.sub.14H.sub.19ClNO [M+H].sup.+: 252.1155, found: 252.1105.

Example 5

Synthesis of Esketamine

[0084] ##STR00069##

[0085] To a solution of methyl amine 6 (230 mg, 0.914 mmol, 1.0 eq.) in THF (5 mL) was added an aqueous HCl solution (2 N, 5.5 mL, 11.0 mmol, 12 eq.). The stirred reaction was heated to 70° C. overnight, diluted with EtOAc and water, and partitioned. The aqueous layer was extracted with EtOAc once. The pH of the aqueous layer was adjusted to 10 with a 30% NaOH aqueous solution and extracted with EtOAc three times. The combined organics were washed with saturated aqueous NH.sub.4Cl once, dried over MgSO.sub.4, concentrated, and purified by silica gel column chromatography (eluted with EtOAc/heptane 1/3) to give esketamine 1 as an off-white solid (201 mg, 93% yield). The enantiomeric excess was determined to be 97.7% by chiral HPLC analysis. [α].sub.D.sup.20=−52.6 (c 2.4, EtOH). M.P. 120° C. .sup.1H NMR (400 MHz, CDCl.sub.3) δ 7.54 (dd, J=7.8, 1.4 Hz, 1H), 7.36 (dd, J=7.8, 1.4 Hz, 1H), 7.31 (td, J=7.6, 1.3 Hz, 1H), 7.23 (td, J=7.6, 1.6 Hz, 1H), 2.83-2.71 (m, 1H), 2.55-2.40 (m, 2H), 2.10 (s, 1H), 2.09 (s, 3H), 2.04-1.94 (m, 1H), 1.91-1.82 (m, 1H), 1.80-1.67 (m, 3H). .sup.13C NMR (100 MHz, CDCl.sub.3) δ 209.2, 137.8, 133.8, 131.2, 129.4, 128.7, 126.6, 70.2, 39.5, 38.6, 29.1, 28.1, 21.9. HRMS (ESI) calcd. for C.sub.13H.sub.16ClNO [M+H].sup.+: 238.0999, found: 238.0993.

Example 6

Synthesis of (S)-norketamine

[0086] ##STR00070##

[0087] To a solution of isocyanate 5 (100 mg, 0.379 mmol, 1.0 eq., prepared as described in Example 3) in THF (1 mL) was added an aqueous HCl solution (3 N, 1.9 mL, 5.69 mmol, 15 eq.). The stirred solution was heated to 70° C. overnight. The reaction solution was then diluted with EtOAc and water. The reaction was partitioned, and the organic layer was extracted with EtOAc once. The pH of the aqueous layer was adjusted to 10 with a 30% NaOH aqueous solution, and the basic aqueous layer was extracted with EtOAc three times. The combined organics were washed with a saturated NH.sub.4Cl aqueous solution once, dried over MgSO.sub.4, concentrated, and purified by silica gel column chromatography (eluted with EtOAc/heptane 1/3) to give (S)-norketamine (62 mg, 74% yield) as alight yellow oil. .sup.1H NMR (400 MHz, CDCl.sub.3) δ 7.68 (d, J=7.8 Hz, 1H), 7.40-7.30 (m, 2H), 7.27-7.23 (m, 1H), 2.80-2.71 (m, 1H), 2.60-2.55 (m, 1H), 2.52-2.40 (m, 1H), 2.06-2.01 (m, 1H), 1.91 (s, 2H), 1.85-1.75 (m, 3H), 1.70-1.64 (m, 1H). .sup.13C NMR (100 MHz, CDCl.sub.3) δ 212.9, 140.4, 133.1, 131.1, 129.0, 128.4, 127.2, 66.5, 41.4, 39.1, 28.5, 22.2.

Example 7

Synthesis of D3-esketamine

[0088] ##STR00071##

[0089] To a slurry of excess LiAlD.sub.4 (158 mg, 3.80 mmol, 2.0 eq.) in THF (5 mL) was added a solution of isocyanate 5 (500 mg, 1.90 mmol, 1.0 eq., prepared as described in Example 3) in THF (5 mL). The reaction suspension was heated to 70° C., stirred for 3 h, cooled to room temperature, and quenched with a 30% NaOH aqueous solution (20 mL). The slurry was heated to 90° C., stirred for 30 min, cooled to room temperature, and diluted with DCM. The reaction was partitioned, and the organic layer was extracted with DCM once. The combined organics were dried over MgSO.sub.4, concentrated, diluted with THF (6 mL), and used for the next step without purification. The THF solution was treated with an aqueous HCl solution (4 N, 6 mL, 23.6 mmol, 12 eq.), heated to 70° C., and stirred overnight. The reaction solution was diluted with EtOAc and water. The reaction was partitioned, and the organic layer was extracted with EtOAc once. The pH of the aqueous layer was adjusted to 10 with a 30% NaOH aqueous solution, and the basic aqueous layer was extracted with EtOAc three times. The combined organics were washed with a saturated NH.sub.4Cl aqueous solution once, dried over MgSO.sub.4, concentrated, and purified by silica gel column chromatography (eluted with EtOAc/heptane 1/5 to 1/1) to give D3-ketamine (264 mg, 58% yield for 2 steps) as an off-white solid. .sup.1H NMR (400 MHz, CDCl.sub.3) δ 7.68 (d, J=7.8 Hz, 1H), 7.40-7.30 (m, 2H), 7.27-7.23 (m, 1H), 2.80-2.71 (m, 1H), 2.60-2.55 (m, 1H), 2.52-2.40 (m, 1H), 2.06-2.01 (m, 1H), 1.91 (s, 2H), 1.85-1.75 (m, 3H), 1.70-1.64 (m, 1H). .sup.13C NMR (100 MHz, CDCl.sub.3) δ 212.9, 140.4, 133.1, 131.1, 129.0, 128.4, 127.2, 66.5, 41.4, 39.1, 28.5, 22.2.

[0090] While the foregoing specification teaches the principles of the present invention, with examples provided for the purpose of illustration, it will be understood that the practice of the invention encompasses all of the usual variations, adaptations and/or modifications as come within the scope of the following claims and their equivalents.

[0091] All documents cited herein are incorporated by reference.