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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387936Generated: October 30, 2026

Water → HCID 58931319, compound

https://huagongshe.com/reaction/387936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Chloro-2-(diethylamine)ethane hydrochlorideHCID 13363—
ReactantPotassium BicarbonateHCID 516893—
ReactantHCID 58930969HCID 58930969—
SolventDimethylformamideHCID 6228—
ProductHCID 58931319HCID 58931319—

Reaction Conditions

Temperature55 °C

Reaction Steps

After dissolving 114 mg of 1-(3-fluorophenyl)-3-{-4-[6-(4-hydroxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy]phenyl}urea in 2 ml of dimethylformamide, there were added 44 mg (ca. 1 equivalent) of 2-chloroethyldiethylamine hydrochloride and 63 mg (2.5 equivalents) of potassium bicarbonate, and the mixture was stirred at 50-60° C. for 16 hours. There were then added 17 mg of 2-chloroethyldiethylamine hydrochloride, 20 mg of potassium bicarbonate and 1 ml of dimethylformamide, and the mixture was stirred overnight at the same temperature. It was then returned to room temperature, water was added, and liquid separation and extraction were performed with ethyl acetate-tetrahydrofuran. The organic layer was washed with water and saturated saline, concentrated and subjected to NH silica gel column chromatography (hexane-ethyl acetate) to obtain 33 mg of a crude solid containing the title compound. This was washed with ethyl acetate to obtain 5 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372981B2
Source datasetuspto-grants-2013_02
ORD IDord-7883d8bd04de473292765f3ea868188f
Source noteuspto-grants-2013_02