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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108314Generated: October 31, 2026

Water → 2-Cyclopropanecarbonyl-7-methoxybenzofuran-4-carboxylic Acid (3-methylpyridin-4-yl)amide

https://huagongshe.com/reaction/1108314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-Methyl-4-pyridinamineHCID 74811—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant2-Cyclopropanecarbonyl-7-methoxybenzofuran-4-carboxylic Acid 4-nitrophenyl EsterHCID 54127706—
SolventDimethylformamideHCID 6228—
Product2-Cyclopropanecarbonyl-7-methoxybenzofuran-4-carboxylic Acid (3-methylpyridin-4-yl)amideHCID 5446248450.5%

Reaction Steps

To a stirred solution of 4-amino-3-methylpyridine (160 mg) in dimethylformamide (10 ml) under an atmosphere of nitrogen was added sodium hexamethyldisilazide (1.0M solution in tetrahydrofuran, 1.5 ml). The reaction mixture was stirred at room temperature for 10 minutes. 2-Cyclopropanecarbonyl-7-methoxy-benzofuran-4-carboxylic acid 4-nitrophenyl ester (280 mg) was then added and stirring continued for 18 h. Water (10 ml) was added and the solvent was removed in vacuo. The residue was dissolved in ethyl acetate (150 ml), washed with water (3×50 ml) and washed with brine (50 ml). The combined aqueous layers were extracted with dichloromethane (2×50 ml), the organic layers were combined, dried over magnesium sulfate, filtered and concentrated in vacuo. Purification by flash chromatography on silica eluting with 5% methanol in dichloromethane followed by trituration with diethyl ether afforded the title compound as an off-white solid (130 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06066657
Source datasetuspto-grants-2000_05
ORD IDord-1cfc993ea2af4642a5d2075b3070aa09
Source noteuspto-grants-2000_05