Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1882935Generated: November 1, 2026

Acetic Acid → HCID 21906201, compound

https://huagongshe.com/reaction/1882935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 21906487HCID 21906487—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetoneHCID 180—
ProductHCID 21906201HCID 21906201114.1%

Reaction Steps

To a stirred suspension of N-(5-chloropyridin-2-yl)-2-[(piperidin-4-ylcarbonyl)amino]benzamide trifluoroacetate (0.4 g, 0.85 mmol) in acetone (6 mL) and 1,2-dichloroethane (10 mL) was added glacial acetic acid (0.2 mL, 3.84 mmol) followed by then sodium triacetoxyborohydride (0.81 g, 3.84 mmol). After stirring for 15 h, saturated aqueous ammonium chloride (10 mL) was added. After stirring for 0.5 h, the mixture was partitioned between dichloromethane and water and the layers separated. The organic phase was washed with saturated aqueous sodium chloride, dried with magnesium sulfate, filtered, and concentrated in vacuo. The residue was then purified by preparative RPHPLC (C18), eluting with a linear gradient of 90/10 to 60/40 (0.01% HCl/acetonitrile) over 180 min. The product containing fractions were combined and lyophilized to give 0.212 g (57%) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06759414B2
Source datasetuspto-grants-2004_07
ORD IDord-90db422444b249ce9e8816a64f3ea27e
Source noteuspto-grants-2004_07