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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510849Generated: October 29, 2026

Ammonium Acetate → Dimethyl[6-(1-aminoethyl)-4-chloro-3'-fluoro-3-methylbiphenyl-2-yl]imidodicarbonate

https://huagongshe.com/reaction/510849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantDimethyl (6-acetyl-4-chloro-3'-fluoro-3-methylbiphenyl-2-yl)imidodicarbonateHCID 86666778—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
ProductDimethyl[6-(1-aminoethyl)-4-chloro-3'-fluoro-3-methylbiphenyl-2-yl]imidodicarbonateHCID 86666779—

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of dimethyl (6-acetyl-4-chloro-3′-fluoro-3-methylbiphenyl-2-yl)imidodicarbonate (67 mg, 0.17 mmol), ammonium acetate (131 mg, 1.70 mmol) and sodium cyanoborohydride (21 mg, 0.34 mmol) in methanol (0.6 mL) and acetonitrile (0.6 mL) was heated at 65° C. overnight in a sealed tube. The mixture was then cooled to room temperature and quenched with saturated sodium bicarbonate and extracted with dichloromethane. The combined extracts were dried over magnesium sulfate and evaporated to dryness. The crude product was used directly in next step (67 mg, 100%). LCMS calculated for C19H21ClFN2O4 (M+H)+: m/z=395.1. found: 395.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096600B2
Source datasetuspto-grants-2015_08
ORD IDord-000e9c4f2cd145f9b03e0f9f93a57e76
Source noteuspto-grants-2015_08