Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365862Generated: November 2, 2026

Trifluoroacetic acid → HCID 22872664, compound

https://huagongshe.com/reaction/365862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 22872663HCID 22872663—
SolventDichloromethaneHCID 6344—
ProductHCID 22872664HCID 22872664—

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 numberUS06127386
Source datasetuspto-grants-2000_10
ORD IDord-1f5c661aa2824fa095d895e33bf842a9
Source noteuspto-grants-2000_10