Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510865Generated: October 31, 2026

Ammonium Acetate → 6-(1-Aminoethyl)-4-chloro-3',5'-difluoro-3-methylbiphenyl-2-carboxamide

https://huagongshe.com/reaction/510865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant6-Acetyl-4-chloro-3',5'-difluoro-3-methylbiphenyl-2-carboxamideHCID 86666794—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
Product6-(1-Aminoethyl)-4-chloro-3',5'-difluoro-3-methylbiphenyl-2-carboxamideHCID 88540650—

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 6-acetyl-4-chloro-3′,5′-difluoro-3-methylbiphenyl-2-carboxamide (61 mg, 0.19 mmol), ammonium acetate (150 mg, 1.9 mmol) and sodium cyanoborohydride (24 mg, 0.38 mmol) in methanol (0.7 mL) and acetonitrile (0.7 mL) was heated at 65° C. overnight in a sealed tube. The mixture was then cooled to room temperature, quenched with saturated sodium bicarbonate and extracted with ethyl acetate. The combined extracts were dried over magnesium sulfate and evaporated to dryness. The crude product was used directly in next step (61 mg, 99%). LCMS calculated for C16H13ClF2NO (M−NH2)+: m/z=308.1. found: 308.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096600B2
Source datasetuspto-grants-2015_08
ORD IDord-104a774647d34b5087789a77a922fdd0
Source noteuspto-grants-2015_08