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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092201Generated: October 30, 2026

Ethyl Acetate → HCID 11996232, compound

https://huagongshe.com/reaction/1092201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantFormamidine acetateHCID 160693—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67478851HCID 67478851—
SolventEthanolHCID 702—
ProductHCID 11996232HCID 1199623250.6%

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of (S)-N3-(5-cyclopropyl-1H-pyrazol-3-yl)-N1-[1-(4-fluorophenyl)ethyl]benzene-1,3,4-triamine (Method 62; 0.395 g, 1.12 mmol) and formamidine acetate (0.234 g, 2.25 mmol) in EtOH (5 ml) was heated at reflux for 2 hrs. After cooling to 25° C., the reaction mixture was treated with saturated sodium bicarbonate solution (10 ml) and EtOAc (30 ml). The organic layer was separated, washed with brine (10 ml), and dried over Na2SO4. The solvent was removed under reduced pressure and the residue was purified by column chromatography (EtOAc) to give the title compound as an off-white solid (0.205 g, 50%). NMR (400 MHz) 12.65 (s, 1H), 8.17 (s, 1H), 7.43 (m, 2H), 7.33 (d, J=8.8 Hz, 1H), 7.10 (m, 2H), 6.90 (s, 1H), 6.62 (d, J=8.8 Hz, 1H), 6.25 (d, J=6.4 Hz, 1H), 6.08 (s, 1H), 4.51 (m, 1H), 1.96 (m, 1H), 1.43 (d, J=6.8 Hz, 3H), 1.02 (m, 2H), 0.76 (m, 2H). MS: Calcd.: 361; Found: [M+H]+ 362.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129403B2
Source datasetuspto-grants-2012_03
ORD IDord-98190e1a4e024a5fa47efe212780f088
Source noteuspto-grants-2012_03