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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414390Generated: November 4, 2026

HCID 23533837, compound → HCID 12148457, compound

https://huagongshe.com/reaction/2414390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23533837HCID 23533837—
SolventFormic AcidHCID 284—
ProductHCID 12148457HCID 12148457—

Reaction Steps

N-[2-[3-(allyloxycarbonyl)-benzyloxy]-1(S)-cyanoethyl]-3-methyl-Nα-(t-butoxycarbonyl)-L-phenylalaninamide (4.36 g, 8.37 mmol) in formic acid (47 mL) is stirred at room temp. for 6 h, after which time the formic acid is evaporated at 25° C. The residue is then dissolved in water (50 mL), basified with sat'd aqueous NaHCO3, and extracted with ethyl acetate (3×50 mL). The combined organic layers are then washed with water (50 mL), brine (50 mL), dried (MgSO4) and evaporated to yield N-[2-[3-(allyloxycarbonyl)-benzyloxy]-1(S)-cyanoethyl]-3-methyl-L-phenylalaninamide, as a clear oil, which is utilized without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06812237B2
Source datasetuspto-grants-2004_11
ORD IDord-eaeaa65bdc084c3b9cb1a8ba9c6f6b93
Source noteuspto-grants-2004_11