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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402539Generated: October 30, 2026

Acetic Acid → HCID 71293539, compound

https://huagongshe.com/reaction/1402539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTetrahydrofuranHCID 8028—
Reactant1-Piperazinecarboxylic acid, ethyl esterHCID 8431—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 71543002HCID 71543002—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 71293539HCID 71293539—

Reaction Steps

To a stirred solution of 5-{4-[3-fluoro-4-({[(2-fluoro-5-methylphenyl)amino]carbonyl}amino)phenoxy]pyridin-2-yl}-N-(2-oxoethyl)-1H-pyrrole-3-carboxamide (200 mg, 0.40 mmol) and 1-ethoxycarbonylpiperazine (158 mg, 1.0 mmol) in anhydrous DMF (10 ml) was added acetic acid (10 mg, 0.17 mmol). The mixture was stirred under nitrogen for 60 minutes, followed by addition of 1M sodium cyanoborohydride solution in THF (1.0 ml, 1.0 mmol). The reaction mixture was stirred for another hour, and poured into 100 ml of water with vigorous stirring. The precipitates were filtered, washed with water, and dried in vacuo to give the crude, which was purified by silica gel chromatography eluting with 5% methanol/chloroform solution to give ethyl 4-(2-{[(5-{4-[3-fluoro-4-({[(2-fluoro-5-methylphenyl)amino]carbonyl}amino)phenoxy]pyridin-2-yl}-1H-pyrrol-3-yl)carbonyl]amino}ethyl)piperazine-1-carboxylate as white solid. Yield: 77 mg, 30%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906944B2
Source datasetuspto-grants-2014_12
ORD IDord-75f3a6337d9149c6acb52b65446f0fdd
Source noteuspto-grants-2014_12