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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572661Generated: November 1, 2026

Acetoxyacetyl chloride → HCID 86675917, compound

https://huagongshe.com/reaction/572661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoxyacetyl chlorideHCID 26297—
ReactantHCID 71466164HCID 71466164—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 86675917HCID 8667591790%

Reaction Steps

To a cold solution of N-(4-fluoro-3-methoxybenzyl)-2-methyl-6-(5-(piperidin-4-yl)-4,5-dihydroisoxazol-3-yl)pyrimidine-4-carboxamide hydrochloride (1.8 g, 3.87 mmol, Preparation #K.1) in dichloromethane (20 mL) were added TEA (3.3 mL, 23.2 mmol) and acetoxyacetyl chloride (0.5 mL, 4.65 mmol). The reaction mixture was slowly warmed to RT and stirred for about 10 min. The reaction mixture was diluted with water (10 mL) and the product was extracted with DCM (2×20 mL). The combined organic layers were washed with water (1×25 mL) followed by brine (1×50 mL). The organic layer was dried over sodium sulphate and concentrated under reduced pressure to afford 2-(4-(3-(6-(4-fluoro-3-methoxybenzylcarbamoyl)-2-methylpyrimidin-4-yl)-4,5-dihydroisoxazol-5-yl)piperidin-1-yl)-2-oxoethyl acetate as a brown solid 1.8 g (90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029409B2
Source datasetuspto-grants-2015_05
ORD IDord-c7a915ae12bf41aa8991dfdf854a59fd
Source noteuspto-grants-2015_05