Carbamic acid, [(1S,2S)-3-[[(1S)-2-amino-1-[(4-bromophenyl)methyl]-2-oxoethyl]amino] -2-hydroxy-1-(phenylmethyl)propyl]-, 1,1-dimethylethyl ester

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Chemical Name:Carbamic acid, [(1S,2S)-3-[[(1S)-2-amino-1-[(4-bromophenyl)methyl]-2-oxoethyl]amino] -2-hydroxy-1-(phenylmethyl)propyl]-, 1,1-dimethylethyl ester
CAS No.:500767-17-9
Molecular Formula:C24H32BrN3O4
Molecular Weight:506.44
Hs Code.:

Carbamic acid,
[(1S,2S)-3-[[(1S)-2-amino-1-[(4-bromophenyl)methyl]-2-oxoethyl]amino]
-2-hydroxy-1-(phenylmethyl)propyl]-, 1,1-dimethylethyl ester

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Chemical Property of Carbamic acid, [(1S,2S)-3-[[(1S)-2-amino-1-[(4-bromophenyl)methyl]-2-oxoethyl]amino] -2-hydroxy-1-(phenylmethyl)propyl]-, 1,1-dimethylethyl ester

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Technology Process of Carbamic acid, [(1S,2S)-3-[[(1S)-2-amino-1-[(4-bromophenyl)methyl]-2-oxoethyl]amino] -2-hydroxy-1-(phenylmethyl)propyl]-, 1,1-dimethylethyl ester

There total 3 articles about Carbamic acid, [(1S,2S)-3-[[(1S)-2-amino-1-[(4-bromophenyl)methyl]-2-oxoethyl]amino] -2-hydroxy-1-(phenylmethyl)propyl]-, 1,1-dimethylethyl 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: 62.0%

: 98760-08-8
(2R,3S)-3-[N-(tert-butyloxycarbonyl)amino]-1,2-epoxy-4-phenylbutane

: 500767-10-2
(2S)-2-amino-3-(4-bromophenyl)propanamide

: 500767-17-9
(2S,5S,6S)-3-aza-2-(p-bromobenzyl)-6-[(tert-butyloxycarbonyl)amino]-5-hydroxy-7-phenylheptanoyl amide

Guidance literature:: In isopropyl alcohol; Heating;
DOI:10.1021/jm020951i

Reference yield:

: 24250-84-8
H-p-BrPhe-OH

: 500767-17-9
(2S,5S,6S)-3-aza-2-(p-bromobenzyl)-6-[(tert-butyloxycarbonyl)amino]-5-hydroxy-7-phenylheptanoyl amide

Guidance literature:: Multi-step reaction with 3 steps

1: AcCl / 20 °C

2: 1.96 g / NH₃ / methanol

3: 62 percent / propan-2-ol / Heating

With ammonia; acetyl chloride; In methanol; isopropyl alcohol;
DOI:10.1021/jm020951i

Reference yield:

: 99359-33-8
(S)-methyl 2-amino-3-(4-bromophenyl)propanoate

: 500767-17-9
(2S,5S,6S)-3-aza-2-(p-bromobenzyl)-6-[(tert-butyloxycarbonyl)amino]-5-hydroxy-7-phenylheptanoyl amide

Guidance literature:: Multi-step reaction with 2 steps

1: 1.96 g / NH₃ / methanol

2: 62 percent / propan-2-ol / Heating

With ammonia; In methanol; isopropyl alcohol;
DOI:10.1021/jm020951i