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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774616Generated: November 2, 2026

Trifluoroacetic acid → HCID 117684692, compound

https://huagongshe.com/reaction/1774616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 117684691HCID 117684691—
SolventDichloromethaneHCID 6344—
ProductHCID 117684692HCID 11768469292%

Reaction Steps

Trifluoroacetic acid (6 ml) was added dropwise to a stirred solution of methyl (2S)-2-{[(tert-butoxy)carbonyl]amino}-5-[6-(3-chloro-4-cyclopropoxyphenyl)pyrimidin-4-yl]pent-4-ynoate (2.26 g, 4.8 mmol) in dichloromethane (20 ml) and the mixture was stirred at room temperature overnight. After this time the reaction mixture was concentrated and the resulting residue redissolved in DCM (20 ml) before being washed with saturated sodium bicarbonate. The organic layer was separated, dried (MgSO4), filtered and concentrated to give the title compound (1.64 g, 92% yield) as a brown oil. Tr=1.63 min m/z (ES+) (M+H+) 372, 373.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260422B2
Source datasetuspto-grants-2016_02
ORD IDord-db2ed04f5a124a54a4f0d66066b98dcb
Source noteuspto-grants-2016_02