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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658043Generated: October 26, 2026

Ethyl Acetate → N-(2-Aminophenyl)-4-[3-(2,3-dihydrobenzo[1,4]dioxin-6-yl)-1-[3-(4-methylpiperazin-1-yl)propyl]ureidomethyl]benzamide

https://huagongshe.com/reaction/658043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium BicarbonateHCID 516892—
ReactantHydrogen chloride-ethyl acetateHCID 21866389—
ReactantN-(2-t-Butoxycarbonylaminophenyl)-4-[3-(2,3-dihydrobenzo[1,4]dioxin-6-yl)-1-[3-(4-methylpiperazin-1-yl)propyl]ureidomethyl]benzamideHCID 58000978—
SolventMethanolHCID 887—
ProductN-(2-Aminophenyl)-4-[3-(2,3-dihydrobenzo[1,4]dioxin-6-yl)-1-[3-(4-methylpiperazin-1-yl)propyl]ureidomethyl]benzamideHCID 5800126882%

Reaction Steps

4.0 M hydrogen chloride ethyl acetate solution (10 mL) was added to a solution of N-(2-t-butoxycarbonylaminophenyl)-4-[3-(2,3-dihydrobenz o[1,4]dioxin-6-yl)-1-[3-(4-methylpiperazine-1-yl)propyl]ureidomethyl]benzamide (Reference Compound No. 13-1, 450 mg, 0.68 mmol) in a mixed solvent (ethyl acetate (10 mL) and methanol (10 mL)), and then the mixture was stirred at room temperature for 2.5 hours. Saturated aqueous sodium hydrogen carbonate solution (150 mL) was added thereto, the whole was extracted with chloroform (150 mL), and then the organic layer was washed with brine (150 mL). The organic layer was dried over anhydrous sodium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (NH-modified silica gel, chloroform-methanol) to give 310 mg of the title compound as a colorless amorphous product. (Yield 82%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076332B2
Source datasetuspto-grants-2011_12
ORD IDord-6b293b65c8e14d3f87e962ac82638422
Source noteuspto-grants-2011_12