Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | HCID 15168934 | HCID 15168934 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15168935 | HCID 15168935 | 79.3% |
Reaction Steps
A mixture of 2-chloro-5-nitro-N-(3-hydroxytol-4-yl)-3-pyridinecarboxamide (6.3 g, 0.02 mol) and pyridine (100 ml) was heated under argon at 90° C. for 2.5 hours. The cooled solution was diluted with water and the yellow-orange precipitate collected and washed with water. The solid was then stirred in hot water (100 ml) for 45 min., filtered and washed with ethanol and ether to give 4.3 g of a tan-brown solid. Recrystallization from dimethylformamide/water afforded 3.76 g (69% of theory) of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05550122 |
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| Source dataset | uspto-grants-1996_08 |
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| ORD ID | ord-b60f204d8643434ca12004f710475706 |
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| Source note | uspto-grants-1996_08 |
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