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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305145Generated: October 29, 2026

Trifluoroacetic acid → HCID 22872628, compound

https://huagongshe.com/reaction/2305145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 22872663HCID 22872663—
SolventDichloromethaneHCID 6344—
ProductHCID 22872628HCID 22872628—

Reaction Conditions

Temperature0 °C

Reaction Steps

5-benzoyl-6-chloro-3-(1-BOC-2-(S)-azetidinylmethoxy)pyridine from step 107a is dissolved in CH2Cl2 (10 mL). The mixture is cooled to 0° C., TFA (10 mL) is added and the reaction is stirred for 45 minutes as it warms to room temperature. The mixture is concentrated in vacuo and taken up in a minimum amount of H2O. The aqueous mixture is basified with 15% NaOH and extracted with CH2Cl2 (200 mL), which is dried (MgSO4) and concentrated. The residue is chromatographed (silica gel) to afford the free amine. The isolated free amine is taken up in a minimum amount of Et2O, cooled to 0° C., and treated with HCl in EtOH to afford the hydrochloride salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06437138B1
Source datasetuspto-grants-2002_08
ORD IDord-ad8b373d3d4d414a97dac6512f024afd
Source noteuspto-grants-2002_08