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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619064Generated: November 1, 2026

Pyridine → HCID 89832359, compound

https://huagongshe.com/reaction/1619064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
ReactantHCID 86762236HCID 86762236—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 89832359HCID 8983235985.1%

Reaction Conditions

Temperature58 °C

Reaction Steps

To a stirred solution of the N-[7a-(5-fluoro-2-thienyl)-6-pyrimidin-2-yl-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-2-yl]benzamide (100 mg, 0.228 mmol) in ethanol (4.6 mL) is added pyridine (0.184 mL, 2.28 mmol) and O-methylhydroxylamine hydrochloride (190 mg, 2.28 mmol). The resulting mixture is heated at 58° C. for 15 hours. The solution is allowed to cool to room temperature, diluted with ethyl acetate (25 mL), and washed with dilute sodium bicarbonate ((20 mL) prepared from water (10 mL) and saturated sodium bicarbonate (10 mL)). The aqueous phase is extracted with ethyl acetate (25 mL). The combined organic extracts are dried over sodium sulfate, filtered, and concentrated. The residue is purified by silica gel flash chromatography eluting with dichloromethane/7 M ammonia in methanol, gradient from 99:1 to 95:5, to give the title compound (65 mg, 0.194 mmol, 85%) as a white solid. ES/MS (m/e): 336 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772282B2
Source datasetuspto-grants-2014_07
ORD IDord-896263ba1d534591a7a2482c86df3b73
Source noteuspto-grants-2014_07