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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092212Generated: November 2, 2026

Ethyl Acetate → 3-(5-Cyclopropyl-1H-pyrazol-3-yl)-4,6-difluoro-N-((S)-1-(4-fluorophenyl)ethyl)-3H-benzo[d]imidazol-5-amine

https://huagongshe.com/reaction/1092212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantFormamidine acetateHCID 160693—
ReactantSodium BicarbonateHCID 516892—
Reactant(S)-N3-(5-Cyclopropyl-1H-pyrazol-3-yl)-2,6-difluoro-N1-(1-(4-fluorophenyl)ethyl)benzene-1,3,4-triamineHCID 86621763—
SolventEthanolHCID 702—
Product3-(5-Cyclopropyl-1H-pyrazol-3-yl)-4,6-difluoro-N-((S)-1-(4-fluorophenyl)ethyl)-3H-benzo[d]imidazol-5-amineHCID 66589200—

Reaction Steps

(S)-N3-(5-Cyclopropyl-1H-pyrazol-3-yl)-2,6-difluoro-N1-(1-(4-fluorophenyl)ethyl)benzene-1,3,4-triamine (Method 101, 0.278 g, 0.718 mmol) and formamidine acetate (0.149 g, 1.44 mmol) in EtOH (10 ml) was heated at reflux for 1 hour. Saturated sodium bicarbonate solution (5 ml) and EtOAc (15 ml) were added. The organic layer was separated, washed with brine (3 ml) and dried over sodium sulfate. The solvent was removed under reduced pressure and the residue was purified by chromatography (Hex-EtOAc=1:1) to give the title compound as off white solid (0.120 g, 42%). 1H NMR (400 MHz) 12.83 (s, 1H), 8.20 (s, 1H), 7.36 (m, 2H), 7.31 (d, J=11.2 Hz, 1H), 7.06 (t, J=8.8 Hz, 2H), 6.15 (s, 1H), 5.15 (d, J=10.4 Hz, 1H), 4.67 (m, 1H), 1.98 (m, 1H), 1.46 (d, J=6.8 Hz, 3H), 1.00 (m, 2H), 0.76 (m, 2H). MS: Calcd.: 397; Found: [M+H]+ 398.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129403B2
Source datasetuspto-grants-2012_03
ORD IDord-fe9214a35ade4953a6de62f03e2bbfa6
Source noteuspto-grants-2012_03