2-(S)-tert-butoxycarbonylamino-3-thiocarbamoyl-propionic acid benzyl ester

Base Information

Chemical Name:2-(S)-tert-butoxycarbonylamino-3-thiocarbamoyl-propionic acid benzyl ester
CAS No.:1312304-07-6
Molecular Formula:C₁₆H₂₂N₂O₄S
Molecular Weight:338.428
Hs Code.:

Synonyms:2-(S)-tert-butoxycarbonylamino-3-thiocarbamoyl-propionic acid benzyl ester

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Chemical Property of 2-(S)-tert-butoxycarbonylamino-3-thiocarbamoyl-propionic acid benzyl ester

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Technology Process of 2-(S)-tert-butoxycarbonylamino-3-thiocarbamoyl-propionic acid benzyl ester

There total 1 articles about 2-(S)-tert-butoxycarbonylamino-3-thiocarbamoyl-propionic acid benzyl 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:

: 13512-57-7
N-[(1,1-dimethylethoxycarbonyl)amino]-L-asparagine benzyl ester

: 1312304-07-6
2-(S)-tert-butoxycarbonylamino-3-thiocarbamoyl-propionic acid benzyl ester

Guidance literature:: With Lawessons reagent; hydrazine; In tetrahydrofuran; at 20 ℃; for 72h;

Reference yield:

: bromoacetate diethylacetal

: 1312304-07-6
2-(S)-tert-butoxycarbonylamino-3-thiocarbamoyl-propionic acid benzyl ester

: 1312304-08-7
2-(S)-tert-butoxycarbonylamino-3-thiazol-2-yl-propionic acid benzyl ester

Guidance literature:: In 1,2-dimethoxyethane; for 3h; Reflux;

Reference yield:

: 1312304-07-6
2-(S)-tert-butoxycarbonylamino-3-thiocarbamoyl-propionic acid benzyl ester

: 1312304-13-4
(1-{3-[5-(3,4-dimethoxy-phenylcarbamoyl)-1H-indol-2-yl]-propylcarbamoyl}-2-thiazol-2-yl-ethyl)-(S)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 1,2-dimethoxyethane / 3 h / Reflux

2: water; lithium hydroxide / tetrahydrofuran / 6 h / 20 °C

3: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 24 h / 20 °C

With water; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; lithium hydroxide; In tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane;