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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780251Generated: November 2, 2026

2-(3-{[(Benzyloxy)carbonyl]amino}phenoxy)acetic acid → 1-{(2S,3S)-3-[N2-(3-Benzyloxycarbonylaminophenoxy)acetyl-L--asparaginyl]amino-2-hydroxy-4-phenylbutyryl}-N-t-butyl-L-prolinamide

https://huagongshe.com/reaction/1780251

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-{[(Benzyloxy)carbonyl]amino}phenoxy)acetic acidHCID 18957386—
Reactant1-[(2S,3S)-3-L-asparaginylamino-2-hydroxy-4-phenylbutyryl]-N-t-butyl-L-prolinamide hydrochlorideHCID 67722782—
Product1-{(2S,3S)-3-[N2-(3-Benzyloxycarbonylaminophenoxy)acetyl-L--asparaginyl]amino-2-hydroxy-4-phenylbutyryl}-N-t-butyl-L-prolinamideHCID 8675082250.2%

Reaction Steps

Following a procedure similar to that described in Example 14, but using 0.45 g (0.91 mmol) of 1-[(2S,3S)-3-L-asparaginylamino-2-hydroxy-4-phenylbutyryl]-N-t-butyl-L-prolinamide hydrochloride and 0.30 g (1.00 mmol) of 3-benzyloxycarbonylaminophenoxyacetic acid, 0.34 g of the title compound were obtained as a colorless powder, melting at 107°-117° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05629406
Source datasetuspto-grants-1997_05
ORD IDord-1594ba3e8e6e495c9513ad7386328805
Source noteuspto-grants-1997_05