HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572661Generated: November 1, 2026
Acetoxyacetyl chloride → HCID 86675917, compound
https://huagongshe.com/reaction/572661
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetoxyacetyl chloride | HCID 26297 | — |
| Reactant | HCID 71466164 | HCID 71466164 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86675917 | HCID 86675917 | 90% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029409B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-c7a915ae12bf41aa8991dfdf854a59fd |
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| Source note | uspto-grants-2015_05 |
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