[(R)-(2-Benzyloxy-4-methoxy-phenyl)-((1S,2R)-2-(3-chloro-4-fluoro-5-nitro-phenyl)-1-{[(S)-(3,5-dimethoxy-phenyl)-methylcarbamoyl-methyl]-carbamoyl}-2-hydroxy-ethylcarbamoyl)-methyl]-carbamic acid tert-butyl ester

Base Information

• Chemical Name: [(R)-(2-Benzyloxy-4-methoxy-phenyl)-((1S,2R)-2-(3-chloro-4-fluoro-5-nitro-phenyl)-1-{[(S)-(3,5-dimethoxy-phenyl)-methylcarbamoyl-methyl]-carbamoyl}-2-hydroxy-ethylcarbamoyl)-methyl]-carbamic acid tert-butyl ester
• CAS No.: 218902-11-5
• Molecular Formula: C₄₁H₄₅ClFN₅O₁₂
• Molecular Weight: 854.286

Synonyms:[(R)-(2-Benzyloxy-4-methoxy-phenyl)-((1S,2R)-2-(3-chloro-4-fluoro-5-nitro-phenyl)-1-{[(S)-(3,5-dimethoxy-phenyl)-methylcarbamoyl-methyl]-carbamoyl}-2-hydroxy-ethylcarbamoyl)-methyl]-carbamic acid tert-butyl ester

Chemical Property of [(R)-(2-Benzyloxy-4-methoxy-phenyl)-((1S,2R)-2-(3-chloro-4-fluoro-5-nitro-phenyl)-1-{[(S)-(3,5-dimethoxy-phenyl)-methylcarbamoyl-methyl]-carbamoyl}-2-hydroxy-ethylcarbamoyl)-methyl]-carbamic acid tert-butyl ester

Chemical Property:

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Technology Process of [(R)-(2-Benzyloxy-4-methoxy-phenyl)-((1S,2R)-2-(3-chloro-4-fluoro-5-nitro-phenyl)-1-{[(S)-(3,5-dimethoxy-phenyl)-methylcarbamoyl-methyl]-carbamoyl}-2-hydroxy-ethylcarbamoyl)-methyl]-carbamic acid tert-butyl ester

There total 10 articles about [(R)-(2-Benzyloxy-4-methoxy-phenyl)-((1S,2R)-2-(3-chloro-4-fluoro-5-nitro-phenyl)-1-{[(S)-(3,5-dimethoxy-phenyl)-methylcarbamoyl-methyl]-carbamoyl}-2-hydroxy-ethylcarbamoyl)-methyl]-carbamic acid tert-butyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

(2-benzyloxy-4-methoxy-phenyl)-tert-butoxycarbonylamino-acetic acid + (2S,3R)-2-Amino-3-(3-chloro-4-fluoro-5-nitro-phenyl)-N-[(S)-(3,5-dimethoxy-phenyl)-methylcarbamoyl-methyl]-3-hydroxy-propionamide → [(R)-(2-Benzyloxy-4-methoxy-phenyl)-((1S,2R)-2-(3-chloro-4-fluoro-5-nitro-phenyl)-1-{[(S)-(3,5-dimethoxy-phenyl)-methylcarbamoyl-methyl]-carbamoyl}-2-hydroxy-ethylcarbamoyl)-methyl]-carbamic acid tert-butyl ester (218902-11-5)

Guidance literature:

With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; at 0 ℃; Yield given;

DOI:10.1002/(SICI)1521-3773(19981016)37:19<2700::AID-ANIE2700>3.0.CO;2-P

Reference yield:

3-chloro-4-fluoro-5-nitro-benzaldehyde → [(R)-(2-Benzyloxy-4-methoxy-phenyl)-((1S,2R)-2-(3-chloro-4-fluoro-5-nitro-phenyl)-1-{[(S)-(3,5-dimethoxy-phenyl)-methylcarbamoyl-methyl]-carbamoyl}-2-hydroxy-ethylcarbamoyl)-methyl]-carbamic acid tert-butyl ester (218902-11-5)

Guidance literature:

Multi-step reaction with 8 steps

1: 1.) Sn(OTf)2, N-ethylpiperidine / 1.) THF, -78 deg C

2: DMAP / CH₂Cl₂

3: HCO₂H, H₂O₂ / H₂O

4: LiOOH / -5 °C

5: EDCI*HCl, HOBt / CH₂Cl₂; dimethylformamide / 0 °C

6: Li₂CO₃ / methanol / Ambient temperature

7: TFA, Me₂S / CH₂Cl₂ / 0 °C

8: EDCI*HCl, HOBt / tetrahydrofuran / 0 °C

With 1-ethyl-piperidine; dmap; tin(II) trifluoromethanesulfonate; formic acid; lithium hydroperoxide; dimethylsulfide; dihydrogen peroxide; lithium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;

DOI:10.1002/(SICI)1521-3773(19981016)37:19<2700::AID-ANIE2700>3.0.CO;2-P

Reference yield:

2-amino-2-(3,5-dimethoxy-phenyl)-N-methyl-acetamide (1026848-12-3) → [(R)-(2-Benzyloxy-4-methoxy-phenyl)-((1S,2R)-2-(3-chloro-4-fluoro-5-nitro-phenyl)-1-{[(S)-(3,5-dimethoxy-phenyl)-methylcarbamoyl-methyl]-carbamoyl}-2-hydroxy-ethylcarbamoyl)-methyl]-carbamic acid tert-butyl ester (218902-11-5)

Guidance literature:

Multi-step reaction with 4 steps

1: EDCI*HCl, HOBt / CH₂Cl₂; dimethylformamide / 0 °C

2: Li₂CO₃ / methanol / Ambient temperature

3: TFA, Me₂S / CH₂Cl₂ / 0 °C

4: EDCI*HCl, HOBt / tetrahydrofuran / 0 °C

With dimethylsulfide; lithium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1002/(SICI)1521-3773(19981016)37:19<2700::AID-ANIE2700>3.0.CO;2-P

upstream raw materials:

2-amino-2-(3,5-dimethoxy-phenyl)-N-methyl-acetamide

(4S,5R)-5-(3-Chloro-4-fluoro-5-nitro-phenyl)-2-oxo-oxazolidine-3,4-dicarboxylic acid 3-tert-butyl ester

(S)-4-Benzyl-3-[(4S,5R)-5-(3-chloro-4-fluoro-5-nitro-phenyl)-2-thioxo-oxazolidine-4-carbonyl]-oxazolidin-2-one

(4S,5R)-4-((S)-4-Benzyl-2-oxo-oxazolidine-3-carbonyl)-5-(3-chloro-4-fluoro-5-nitro-phenyl)-2-oxo-oxazolidine-3-carboxylic acid tert-butyl ester

Downstream raw materials:

C₆₃H₅₇ClF₃N₅O₁₅S

C₆₁H₅₃ClF₃N₅O₁₄S

C₅₈H₄₉ClF₃N₅O₁₄S

C₅₈H₅₂ClN₅O₁₁

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