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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912540Generated: November 2, 2026

Methanol → HCID 59410702, compound

https://huagongshe.com/reaction/912540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantChloroacetyl chlorideHCID 6577—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-methyl-6-(4-(2-(piperidin-4-yl)ethoxy)-3-(trifluoromethyl)phenyl)-1H-imidazo[4,5-c]pyridine-4-carbonitrileHCID 49862146—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
SolventTetrahydrofurane dichloromethaneHCID 21919333—
ProductHCID 59410702HCID 59410702—

Reaction Steps

Chloroacetylchloride (0.323 ml) in 1 ml DCM was added at 0° C. to the suspension of 1-methyl-6-(4-(2-(piperidin-4-yl)ethoxy)-3-(trifluoromethyl)phenyl)-1H-imidazo[4,5-c]pyridine-4-carbonitrile (free base) in THF/DCM (1:1, 40 ml) with DIPEA (1.7 ml). The mixture was stirred at rt for 2 hours, then 10 ml methanol added, followed by 200 ml ethyl acetate. The mixture was washed with water (100 ml), sodium bicarbonate (100 ml), dried, filtered, solvent removed, residue was columned on silica gel using 100:5 DCM/MeOH as eluant to give 0.7 g product as off white solid. 1H NMR (CD3OD) δ: 8.25 (d, 1H), 8.22 (s, 1H), 8.10 (s, 1H), 7.87 (s, 1H), 7.10 (d, 1H), 4.58 (m, 1H), 4.21 (t, 2H), 4.09 (d, 1H), 4.08 (d, 1H), 3.99 (s, 3H), 3.90 (m, 1H), 3.12 (t, 1H), 2.65 (t, 1H), 2.2 (m, 1H), 1.8-2.0 (m, 4H), 1.1-1.4 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026236B2
Source datasetuspto-grants-2011_09
ORD IDord-11326172a5d542a7a9e9ef31d053a282
Source noteuspto-grants-2011_09