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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2392957Generated: October 25, 2026

benzyl (2S)-2-aminopropanoate → N-[3-acetylthio-2-(1-indanyl)-1-oxopropyl)alanine benzyl ester

https://huagongshe.com/reaction/2392957

Reaction equation

Participants

RoleNameHCIDCharge
Reactantbenzyl (2S)-2-aminopropanoateHCID 726858—
Reactant3-Acetylthio-2-(1-indanyl)propanoic acidHCID 18793868—
ProductN-[3-acetylthio-2-(1-indanyl)-1-oxopropyl)alanine benzyl esterHCID 5365920972%

Reaction Steps

Using the procedure described in Example 60, but starting with 3-acetylthio-2-(1-indanyl)propanoic acid and alanine benzyl ester, N-[3-acetylthio-2-(1-indanyl)-1-oxopropyl]alanine benzyl ester is obtained in a 72% yield in the form of a white solid, having the following characteristics: m.p.: 95° C.; Rf =0.17 [cyclohexane/ethyl acetate (4:1 by volume)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05801274
Source datasetuspto-grants-1998_09
ORD IDord-a6e48488bc3a4c4f8e6fb36c38e12b89
Source noteuspto-grants-1998_09