HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564729Generated: October 31, 2026
Sodium hydride → 2-Acetyl-7-methoxyfuro[2,3-c]pyridine4-carboxylic acid (3,5-dichloropyridin-4-yl)amide
https://huagongshe.com/reaction/564729
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Amino-3,5-dichloropyridine | HCID 89888 | — |
| Reactant | 2-Acetyl-7-methoxyfuro[2,3-c]pyridine-4-carboxylic acid 4-nitrophenyl ester | HCID 54165983 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Acetyl-7-methoxyfuro[2,3-c]pyridine4-carboxylic acid (3,5-dichloropyridin-4-yl)amide | HCID 9799994 | 11.2% |
Reaction Steps
A solution of 4-amino-3,5-dichloropyridine (57 mg) in dry N,N-dimethylformamide (10 ml) was stirred at room temperature under an atmosphere of dry nitrogen. Sodium hydride (21 mg) was added and stirring continued for 45 minutes. 2-Acetyl-7-methoxyfuro[2,3-c]pyridine-4-carboxylic acid 4-nitrophenyl ester (100 mg) was added and the resulting mixture stirred overnight. The solvent was removed in vacuo, the residue taken up in water (100 ml) and extracted with ethyl acetate (3×100 ml). The combined organic extracts were washed with water (100 ml) then brine (50 ml), dried over magnesium sulfate, filtered and the solvent removed in vacuo. Purification by column chromatography on silica eluting with 50% hexane in ethyl acetate gave the title compound (12 mg) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06169090A |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-d43e9da2ff5742ddbcfef6d11021c5b8 |
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| Source note | uspto-grants-2001_01 |
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