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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510831Generated: October 31, 2026

Ammonium Acetate → 6-(1-Aminoethyl)-4-chloro-3-(cyanomethyl)-3'-fluorobiphenyl-2-carbonitrile

https://huagongshe.com/reaction/510831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant6-Acetyl-4-chloro-3-(cyanomethyl)-3'-fluorobiphenyl-2-carbonitrileHCID 58368599—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
Product6-(1-Aminoethyl)-4-chloro-3-(cyanomethyl)-3'-fluorobiphenyl-2-carbonitrileHCID 86666766—

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 6-acetyl-4-chloro-3-(cyanomethyl)-3′-fluorobiphenyl-2-carbonitrile (0.020 g, 0.064 mmol) and ammonium acetate (49 mg, 0.64 mmol) in methanol (0.4 mL) and acetonitrile (0.4 mL) was heated at 65° C. in a sealed tube for 30 min. The mixture was cooled to room temperature and sodium cyanoborohydride (8 mg, 0.13 mmol) was added. The reaction was heated at 65° C. for another 4 hours, cooled to room temperature, 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 (20 mg, 100%). LCMS calculated for C17H14ClFN3 (M+H)+: m/z=314.1. found: 313.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096600B2
Source datasetuspto-grants-2015_08
ORD IDord-a51216f7a1d741b6a8fed90594edfbf4
Source noteuspto-grants-2015_08