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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510823Generated: October 31, 2026

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

https://huagongshe.com/reaction/510823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant6-Acetyl-4-chloro-3'-fluoro-3-methylbiphenyl-2-carboxamideHCID 86666762—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
Product6-(1-Aminoethyl)-4-chloro-3'-fluoro-3-methylbiphenyl-2-carboxamideHCID 86666763—

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 6-acetyl-4-chloro-3′-fluoro-3-methylbiphenyl-2-carboxamide (110 mg, 0.34 mmol) and ammonium acetate (270 mg, 3.4 mmol) in methanol (1.9 mL) and acetonitrile (2.0 mL) was heated at 65° C. in a sealed tube for 30 min. The mixture was cooled and sodium cyanoborohydride (43 mg, 0.69 mmol) was added. The reaction was heated at 65° C. for another 4 hours. The mixture was cooled, quenched with saturated sodium bicarbonate, and extracted with dichloromethane. The combined extracts were dried over magnesium sulfate and evaporated to dryness. The residue was used directly in next step (98 mg, 93%). LCMS calculated for C16H17ClFN2O (M+H)+: m/z=307.1. found: 306.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096600B2
Source datasetuspto-grants-2015_08
ORD IDord-30e473a6244e4fdf9fdcee4984ad9262
Source noteuspto-grants-2015_08