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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 3-Methyl-4-pyridinamine | HCID 74811 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | 2-Cyclopropanecarbonyl-7-methoxybenzofuran-4-carboxylic Acid 4-nitrophenyl Ester | HCID 54127706 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Cyclopropanecarbonyl-7-methoxybenzofuran-4-carboxylic Acid (3-methylpyridin-4-yl)amide | HCID 54462484 | 50.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06066657 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-1cfc993ea2af4642a5d2075b3070aa09 |
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| Source note | uspto-grants-2000_05 |
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