Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248522Generated: October 31, 2026

HCID 18646534, compound → HCID 67827883, compound

https://huagongshe.com/reaction/2248522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18646534HCID 18646534—
ReactantTrifluoroacetic acid methylene chlorideHCID 21863450—
ProductHCID 67827883HCID 6782788375%

Reaction Steps

A solution of N-[m-(p-amidinobenzamido)benzoyl]-3-(t-butoxycarbonyl)-L-alanine methyl ester hydroidide in CH2Cl2 /trifluoroacetic acid is left to stand at room temperature for 3 hours. After removal of the solvent and recrystallization of the residue from ethanol/ether there is obtained (S)-3-[m-(p-amidinobenzamido)benzamido]-3-(methoxycarbonyl)propionic acid trifluoroacetate in the form of a colourless solid. Yield: 75%, m.p. 132°-134° C. (decomposition). MS: 413 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05039805
Source datasetuspto-grants-1991_08
ORD IDord-763cef1c2b0a4d749401a69bc2788936
Source noteuspto-grants-1991_08