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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402609Generated: November 1, 2026

Acetic Acid → HCID 71293500, compound

https://huagongshe.com/reaction/1402609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTetrahydrofuranHCID 8028—
ReactantPiperidin-4-olHCID 79341—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 71542909HCID 71542909—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 71293500HCID 71293500—

Reaction Steps

To a stirred solution of 5-{4-[4-({[(2-fluoro-5-methylphenyl)amino]carbonyl}amino)phenoxy]pyridin-2-yl}-N-(3-oxopropyl)-1H-pyrrole-3-carboxamide (100 mg, 0.20 mmol) in 10 ml of anhydrous DMF were added 4-hydroxypiperidine (30 mg, 0.30 mmol) and acetic acid (10 mg, 0.17 mmol). The mixture was stirred at room temperature for 30 minutes, followed by addition of 1M sodium cyanoborohydride solution in THF (0.30 ml, 0.30 mmol) and stirring was continued for one more hour. The mixture was poured into 100 ml of water. The precipitates were filtered, washed with water and dried to give the crude, which was purified by silica gel flash chromatography eluting with 20% of MeOH in CHCl3 to give 5-{4-[4-({[(2-fluoro-5-methylphenyl)amino]carbonyl}amino)phenoxy]pyridin-2-yl}-N-[3-(4-hydroxypiperidin-1-yl)propyl]-1H-pyrrole-3-carboxamide as white solid. Yield:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906944B2
Source datasetuspto-grants-2014_12
ORD IDord-e7946011b03948379f6d5f45e317f290
Source noteuspto-grants-2014_12