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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630512Generated: November 1, 2026

Acetic Anhydride → 4-Fluoro-3-(2-(3-(methylsulfinyl)-6-(morpholine-4-carbonyl)-1H-indol-1-yl)pyrimidin-5-yl)phenyl acetate

https://huagongshe.com/reaction/630512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant(1-(5-(2-Fluoro-5-hydroxyphenyl)pyrimidin-2-yl)-3-(methylsulfinyl)-1H-indol-6-yl)(morpholino)methanoneHCID 118671888—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
Product4-Fluoro-3-(2-(3-(methylsulfinyl)-6-(morpholine-4-carbonyl)-1H-indol-1-yl)pyrimidin-5-yl)phenyl acetateHCID 118666179—

Reaction Steps

Acetic anhydride (0.18 mL, 1.9 mmol) was added at 0° C. to 264a) (0.45 g, 0.94 mmol) in pyridine (2.0 mL) and the resulting solution was stirred at room temperature for 3 h. The reaction mixture was diluted with cold water and extracted with dichloromethane/methanol (9:1; 3×30 mL). The organic layers were washed with saturated sodium hydrogen carbonate solution (2×20 mL) and brine (20 mL), dried over sodium sulfate and evaporated. The remnant was purified by flash column chromatography [silica; dichloromethane with 1.5% methanol]. Yield: 0.09 g (38% of theory)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315490B2
Source datasetuspto-grants-2016_04
ORD IDord-f218a312769e4a6d8c62c31cd292b86e
Source noteuspto-grants-2016_04