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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936576Generated: November 2, 2026

Trifluoroacetic acid → HCID 178430659, compound

https://huagongshe.com/reaction/1936576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 178430657HCID 178430657—
SolventDichloromethaneHCID 6344—
ProductHCID 178430659HCID 17843065979.9%

Reaction Steps

To a cold (0° C.) solution of 874 mg of 1-(tert-butoxycarbonyl)-5-[N2, N3-bis(benzyloxycarbonyl)guanidino]-4-methylbenzimidazole in 2 mL of methylene chloride is added 2 mL of trifluoroacetic acid. The resulting solution is stirred at room temperature for 30 minutes, then rotary evaporated. The residue is purified by flash column chromatography on silica gel, eluting with 20% methanol/chloroform followed by recrystallization from hexanes/methylene chloride to provide 573 mg of 5-[N2,N3-bis(benzyloxycarbonyl)guanidino]-4-methylbenzimidazole as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06391878B2
Source datasetuspto-grants-2002_05
ORD IDord-19b9334f91ab49038c4cebe58e7fd6f7
Source noteuspto-grants-2002_05