Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437422Generated: October 27, 2026

Ethyl Acetate → HCID 68520585, compound

https://huagongshe.com/reaction/1437422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAcetamidine monohydrochlorideHCID 67170—
ReactantSodium BicarbonateHCID 516892—
Reactant(S)-N6-(5-Cyclopropyl-1H-pyrazol-3-yl)-N2-(1-(4-fluorophenyl)ethyl)pyridine-2,3,6-triamineHCID 68521442—
SolventEthanolHCID 702—
ProductHCID 68520585HCID 6852058543%

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of crude (S)—N6-(5-cyclopropyl-1H-pyrazol-3-yl)-N2-(1-(4-fluorophenyl)ethyl)pyridine-2,3,6-triamine (Method 9; 0.120 g, 0.34 mmol) and acetamidine hydrochloride (0.052 g, 0.55 mmol) in EtOH (5 ml) was heated at reflux overnight. After cooling to 25° C., saturated NaHCO3 solution (10 ml) and EtOAc (30 ml) were added to the reaction mixture. The organic layer was separated, washed with brine (10 ml), dried over Na2SO4, concentrated, and purified by chromatography (EtOAc:MeOH=100:1) to give the title compound as an off-white solid (0.055 g, 43%). NMR (400 MHz, d6-Acetone) 11.14 (br s, 1H), 8.44 (br s, 1H), 7.70 (d, J=8.4 Hz, 1H), 7.44 (m, 2H), 7.11 (m, 2H), 7.00 (br s, 1H), 6.00 (m, 2H), 2.12 (s, 3H), 2.11 (d, J=7.2 Hz, 3H), 0.89 (m, 2H), 0.65 (m, 2H). MS: Calcd.: 376. Found: [M+H]+ 377.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622482B2
Source datasetuspto-grants-2009_11
ORD IDord-383df3ff65ad4d43a4355cbe9435bd6f
Source noteuspto-grants-2009_11