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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402546Generated: November 1, 2026

Water → HCID 71293523, compound

https://huagongshe.com/reaction/1402546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantMethyl bromoacetateHCID 60984—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-(3-aminopropyl)-5-[4-(2-fluoro-5-{[(2-fluoro-5-methylphenyl)amino]carbonyl}phenoxy)pyridin-2-yl]-1H-pyrrole-3-carboxamideHCID 71293544—
ProductHCID 71293523HCID 71293523—

Reaction Conditions

Temperature55 °C

Reaction Steps

To a stirred solution of N-(3-aminopropyl)-5-[4-(2-fluoro-5-{[(2-fluoro-5-methylphenyl)amino]carbonyl}phenoxy)pyridin-2-yl]-1H-pyrrole-3-carboxamide (85 mg, 0.17 mmol) and N,N-diisopropylethylamine (100 mg, 0.78 mmol) in 10 ml of anhydrous DMF was added methyl bromoacetate (100 mg, 0.65 mmol). The mixture was heated at 55° C. for 30 minutes and poured into 100 ml of water with vigorous stirring. The precipitates were filtered and dried in vacuo to give the crude, which was purified by silica gel chromatography eluting with 3˜5% of MeOH in CHCl3 to afford dimethyl 2,2′-({3-[([5-[4-(2-fluoro-5-{[(2-fluoro-5-methylphenyl)amino]carbonyl}phenoxy)pyridin-2-yl]-1H-pyrrol-3-yl]carbonyl)amino]propyl}imino)diacetate as white solid. Yield: 70 mg, 64%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906944B2
Source datasetuspto-grants-2014_12
ORD IDord-a8f7b6d5cc23472cadcafcb4b564aaa1
Source noteuspto-grants-2014_12