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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242803Generated: October 30, 2026

[(S)-1-(4-Cyano-2-phenylaminophenylcarbamoyl)ethyl]carbamic acid tertbutyl ester → [(S)-1-(6-cyano-1-phenyl-1H-benzoimidazol-2-yl)ethyl]carbamic acid tertbutyl ester

https://huagongshe.com/reaction/242803

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[(S)-1-(4-Cyano-2-phenylaminophenylcarbamoyl)ethyl]carbamic acid tertbutyl esterHCID 68157188—
SolventAcetic AcidHCID 176—
Product[(S)-1-(6-cyano-1-phenyl-1H-benzoimidazol-2-yl)ethyl]carbamic acid tertbutyl esterHCID 68157544100%

Reaction Steps

A solution of [(S)-1-(4-cyano-2-phenylaminophenylcarbamoyl)ethyl]carbamic acid tertbutyl ester (750 mg, 1.97 mmol) in AcOH (3 mL) was stirred for 18 h at 80° C. After cooling to RT, volatiles were evaporated under reduced pressure affording [(S)-1-(6-cyano-1-phenyl-1H-benzoimidazol-2-yl)ethyl]carbamic acid tertbutyl ester (1.97 mmol) which was used without any further purification in the following step. LCMS: RT 3.55 min [M+H]+ 363.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-88c97778fcb84cf9b49d96b152335604
Source noteuspto-grants-2014_02