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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248506Generated: October 30, 2026

Trifluoroacetic acid → HCID 67827898, compound

https://huagongshe.com/reaction/2248506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 54549046HCID 54549046—
SolventDichloromethaneHCID 6344—
ProductHCID 67827898HCID 6782789884%

Reaction Steps

A solution of 55 mg of N-[N-[m-[[3-(p-amidinophenyl)-N-(t-butoxycarbonyl)-DL-alanyl]amino]benzoyl]-3-(t-butoxycarbonyl)-L-alanyl]-3-(1-naphthyl)-L-alanine (1:1 epimer) in a mixture of 10 ml of methylene chloride and 5 ml of trifluoroacetic acid is held at room temperature for 2 hours while gassing with argon. After evaporation of the solvent there is obtained N-[N-[m-[[3-(p-amidinophenyl)-DL-alanyl]amino]benzoyl]-L-α-aspartyl]-3-(1-naphthyl)-L-alanine trifluoroacetate (1:2), m.p. 165° C. (dec.) (ethanol/ethyl acetate), yield: 84% of theory, MS: 639 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05039805
Source datasetuspto-grants-1991_08
ORD IDord-97361fdafb1741939e61e780e51c5cf3
Source noteuspto-grants-1991_08