(1S)-Benzyloxycarbonyl-L-valyl-N-[3-ethoxy-2-hydroxy-3-imino-1-(1-methylethyl)propyl]-L-prolinamide hydrochloride

Base Information

Chemical Name:(1S)-Benzyloxycarbonyl-L-valyl-N-[3-ethoxy-2-hydroxy-3-imino-1-(1-methylethyl)propyl]-L-prolinamide hydrochloride
CAS No.:120629-54-1
Molecular Formula:C₂₆H₄₀N₄O₆*ClH
Molecular Weight:541.088
Hs Code.:

Synonyms:(1S)-Benzyloxycarbonyl-L-valyl-N-[3-ethoxy-2-hydroxy-3-imino-1-(1-methylethyl)propyl]-L-prolinamide hydrochloride

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Chemical Property of (1S)-Benzyloxycarbonyl-L-valyl-N-[3-ethoxy-2-hydroxy-3-imino-1-(1-methylethyl)propyl]-L-prolinamide hydrochloride

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Technology Process of (1S)-Benzyloxycarbonyl-L-valyl-N-[3-ethoxy-2-hydroxy-3-imino-1-(1-methylethyl)propyl]-L-prolinamide hydrochloride

There total 3 articles about (1S)-Benzyloxycarbonyl-L-valyl-N-[3-ethoxy-2-hydroxy-3-imino-1-(1-methylethyl)propyl]-L-prolinamide hydrochloride 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:

: 95501-78-3
N-Benzyloxycarbonyl-L-valyl-L-prolyl-L-valinal

: 120629-54-1
(1S)-Benzyloxycarbonyl-L-valyl-N-[3-ethoxy-2-hydroxy-3-imino-1-(1-methylethyl)propyl]-L-prolinamide hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: H₂O / tetrahydrofuran / 4.5 h / Ambient temperature

2: acetyl chloride / CHCl₃ / 16 h / Ambient temperature

With water; acetyl chloride; In tetrahydrofuran; chloroform;
DOI:10.1021/ja00031a046