(R)-4-Carbamoyl-4-{(S)-2-[2-(2-dodecanoylamino-cyclohexyloxy)-acetylamino]-propionylamino}-butyric acid benzyl ester

Base Information

Chemical Name:(R)-4-Carbamoyl-4-{(S)-2-[2-(2-dodecanoylamino-cyclohexyloxy)-acetylamino]-propionylamino}-butyric acid benzyl ester
CAS No.:201684-33-5
Molecular Formula:C₃₅H₅₆N₄O₇
Molecular Weight:644.852
Hs Code.:

Synonyms:(R)-4-Carbamoyl-4-{(S)-2-[2-(2-dodecanoylamino-cyclohexyloxy)-acetylamino]-propionylamino}-butyric acid benzyl ester

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Chemical Property of (R)-4-Carbamoyl-4-{(S)-2-[2-(2-dodecanoylamino-cyclohexyloxy)-acetylamino]-propionylamino}-butyric acid benzyl ester

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Technology Process of (R)-4-Carbamoyl-4-{(S)-2-[2-(2-dodecanoylamino-cyclohexyloxy)-acetylamino]-propionylamino}-butyric acid benzyl ester

There total 4 articles about (R)-4-Carbamoyl-4-{(S)-2-[2-(2-dodecanoylamino-cyclohexyloxy)-acetylamino]-propionylamino}-butyric 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: 70.0%

: 143-07-7
lauric acid

: (R)-4-{(S)-2-[2-(2-Amino-cyclohexyloxy)-acetylamino]-propionylamino}-4-carbamoyl-butyric acid benzyl ester; hydrochloride

: 201684-33-5
(R)-4-Carbamoyl-4-{(S)-2-[2-(2-dodecanoylamino-cyclohexyloxy)-acetylamino]-propionylamino}-butyric acid benzyl ester

Guidance literature:: With diphenyl phosphoryl azide; triethylamine; In N,N-dimethyl-formamide; a) from 0 deg C to 2 deg C, 1 h, b) RT, 60 h;
DOI:10.1021/jm970509d

Reference yield:

: 59524-62-8
L-alanyl-D-isoglutamine benzyl ester hydrochloride

: 201684-33-5
(R)-4-Carbamoyl-4-{(S)-2-[2-(2-dodecanoylamino-cyclohexyloxy)-acetylamino]-propionylamino}-butyric acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 86 percent / diphenyl phosphorazidate, Et₃N / dimethylformamide / a) from 0 deg C to 2 deg C, 1 h, b) RT, 60 h

2: 90 percent / HCl(g), glacial AcOH

3: 70 percent / diphenyl phosphorazidate, Et₃N / dimethylformamide / a) from 0 deg C to 2 deg C, 1 h, b) RT, 60 h

With hydrogenchloride; diphenyl phosphoryl azide; acetic acid; triethylamine; In N,N-dimethyl-formamide;
DOI:10.1021/jm970509d

Reference yield:

: 134962-04-2
trans-2-(2'-t-butyloxycarbonylaminocyclohexyloxy)acetic acid

: 201684-33-5
(R)-4-Carbamoyl-4-{(S)-2-[2-(2-dodecanoylamino-cyclohexyloxy)-acetylamino]-propionylamino}-butyric acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 86 percent / diphenyl phosphorazidate, Et₃N / dimethylformamide / a) from 0 deg C to 2 deg C, 1 h, b) RT, 60 h

2: 90 percent / HCl(g), glacial AcOH

3: 70 percent / diphenyl phosphorazidate, Et₃N / dimethylformamide / a) from 0 deg C to 2 deg C, 1 h, b) RT, 60 h

With hydrogenchloride; diphenyl phosphoryl azide; acetic acid; triethylamine; In N,N-dimethyl-formamide;
DOI:10.1021/jm970509d