(S)-2-[(S)-2-(4-allyloxy-3-chloro-phenyl)-1-methoxycarbonyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:(S)-2-[(S)-2-(4-allyloxy-3-chloro-phenyl)-1-methoxycarbonyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester
CAS No.:1447710-36-2
Molecular Formula:C₂₃H₃₁ClN₂O₆
Molecular Weight:466.962
Hs Code.:

Synonyms:(S)-2-[(S)-2-(4-allyloxy-3-chloro-phenyl)-1-methoxycarbonyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester

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Chemical Property of (S)-2-[(S)-2-(4-allyloxy-3-chloro-phenyl)-1-methoxycarbonyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester

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Technology Process of (S)-2-[(S)-2-(4-allyloxy-3-chloro-phenyl)-1-methoxycarbonyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester

There total 4 articles about (S)-2-[(S)-2-(4-allyloxy-3-chloro-phenyl)-1-methoxycarbonyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic 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: 94.0%

: 15761-39-4,59433-50-0
1-(tert-butoxycarbonyl)-L-proline

: 1447710-23-7
(S)-3-(4-allyloxy-3-chloro-phenyl)-2-amino-propionic acid methyl ester

: 1447710-36-2
(S)-2-[(S)-2-(4-allyloxy-3-chloro-phenyl)-1-methoxycarbonyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 25 ℃; for 20h;

Reference yield:

: 1447710-67-9
(S)-2-(tert-butoxycarbonylamino)-3-(3-chloro-4-hydroxyphenyl)propanoate dicyclohexylammonium salt

: 1447710-36-2
(S)-2-[(S)-2-(4-allyloxy-3-chloro-phenyl)-1-methoxycarbonyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: lithium hydroxide monohydrate / tetrahydrofuran / 20 h / 25 - 80 °C

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 94 h / 40 °C

3: formic acid / 3 h / 20 °C

4: HATU; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 h / 25 °C

With formic acid; lithium hydroxide monohydrate; N-ethyl-N,N-diisopropylamine; HATU; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1447710-21-5
(S)-3-(4-allyloxy-3-chloro-phenyl)-2-tert-butoxycarbonylamino-propionic acid methyl ester

: 1447710-36-2
(S)-2-[(S)-2-(4-allyloxy-3-chloro-phenyl)-1-methoxycarbonyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: formic acid / 3 h / 20 °C

2: HATU; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 h / 25 °C

With formic acid; N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide;