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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376540Generated: October 29, 2026

Trifluoroacetic acid → HCID 70303465, compound

https://huagongshe.com/reaction/376540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantN-HydroxysuccinimideHCID 80170—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 11103621HCID 11103621—
Reactant4-(2-{[(Tert-butoxy)carbonyl]amino}ethyl)benzoic acidHCID 16640905—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventHCID 178418361HCID 178418361—
ProductHCID 70303465HCID 70303465—

Reaction Steps

In 20 ml of methanol was dissolved 300 mg of (S)-3-[3-(4-amidinobenzoylamino)propyl]-4-benzyloxycarbonylaminoacetyl-2-oxopiperazine-1-acetic acid produced in Reference Example 21. To the solution was added 120 mg of 10% Pd--C, and the mixture was stirred for one hour at room temperature in hydrogen streams. The catalyst was filtered off, and the filtrate was concentrated under reduced pressure to give an oily product, which was dissolved in 5 ml of dimethylformamide. To the solution was added 5 ml of activated-ester solution in dimethylformamide which was prepared from 94 mg of N-hydroxysuccinimide and 173 mg of 4-(2-t-butoxycarbonylaminoethyl)benzoic acid in the presence of 167 mg of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride. The mixture was stirred for two hours at room temperature. The reaction mixture was concentrated to give an oily product, which was dissolved in 7 ml of trifluoroacetic acid. The solution was stirred for one hour at room temperature. The reaction mixture was concentrated under reduced pressure to give a crude product, which was purified by means of a CHP-20 column (eluted with 10% acetonitrile/water) to afford 110 mg of the titled compound as a colorless amorphous powdery product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06020334
Source datasetuspto-grants-2000_02
ORD IDord-82287e66446746148c8ede166f4f9905
Source noteuspto-grants-2000_02