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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242867Generated: October 30, 2026

HCID 68157210, compound → HCID 58459222, compound

https://huagongshe.com/reaction/242867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68157210HCID 68157210—
SolventAcetic AcidHCID 176—
ProductHCID 58459222HCID 58459222—

Reaction Steps

A solution of (S)-tert-butyl 1-(5-fluoro-2-(phenylamino)phenylamino)-1-oxopropan-2-ylcarbamate (2.15 mmol) in AcOH (10 mL) was stirred for 18 h at 70° C. After cooling to RT, volatiles were evaporated under reduced pressure and the residue was partitioned between EtOAc and a saturated solution of NaHCO3. The organic layer was washed with brine, dried (MgSO4) and then concentrated in vacuo. The resulting residue was purified by column chromatography (Si—PCC, gradient 0-40% EtOAc in cyclohexane) affording (S)-tert-butyl 1-(5-fluoro-1-phenyl-1H-benzo[d]imidazol-2-yl)ethylcarbamate as an orange oil (661 mg, 86% over two steps). LCMS: RT 3.52 min [M+H]+ 356.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-53265c4394a34be59b17b0e7b29462b2
Source noteuspto-grants-2014_02