(S)-1-((S)-6-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-hexyl)-pyrrolidine-2-carboxylic acid benzyl ester

Base Information

Chemical Name:(S)-1-((S)-6-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-hexyl)-pyrrolidine-2-carboxylic acid benzyl ester
CAS No.:199279-92-0
Molecular Formula:C₃₁H₄₃N₃O₆
Molecular Weight:553.699
Hs Code.:

Synonyms:(S)-1-((S)-6-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-hexyl)-pyrrolidine-2-carboxylic acid benzyl ester

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Chemical Property of (S)-1-((S)-6-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-hexyl)-pyrrolidine-2-carboxylic acid benzyl ester

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Technology Process of (S)-1-((S)-6-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-hexyl)-pyrrolidine-2-carboxylic acid benzyl ester

There total 3 articles about (S)-1-((S)-6-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-hexyl)-pyrrolidine-2-carboxylic 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: 53.0%

: 82689-16-5
benzyl {(5S)-5-[(tert-butoxycarbonyl)amino]-6-oxohexyl}carbamate

: 16652-71-4
benzyl (2S)-2-pyrrolidinecarboxylate hydrochloride

: 199279-92-0
(S)-1-((S)-6-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-hexyl)-pyrrolidine-2-carboxylic acid benzyl ester

Guidance literature:: With sodium cyanoborohydride; acetic acid; In methanol; for 1h;
DOI:10.1021/jm9701132

Reference yield:

: 2389-45-9
Boc-Lys(Z)-OH

: 199279-92-0
(S)-1-((S)-6-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-hexyl)-pyrrolidine-2-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 66 percent / DCC, DMAP, DIPEA / CH₂Cl₂

2: 85 percent / LiAlH₄ / tetrahydrofuran / 0 °C

3: 53 percent / sodium cyanoborohydride, AcOH / methanol / 1 h

With dmap; lithium aluminium tetrahydride; sodium cyanoborohydride; acetic acid; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/jm9701132

Reference yield:

: 130502-06-6
tert-butyl-N-[(1S)-5-(benzyloxycarbonylamino)-1-[methoxy(methyl)carbamoyl]pentyl]carbamate

: 199279-92-0
(S)-1-((S)-6-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-hexyl)-pyrrolidine-2-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / LiAlH₄ / tetrahydrofuran / 0 °C

2: 53 percent / sodium cyanoborohydride, AcOH / methanol / 1 h

With lithium aluminium tetrahydride; sodium cyanoborohydride; acetic acid; In tetrahydrofuran; methanol;
DOI:10.1021/jm9701132