Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | HCID 15636996 | HCID 15636996 | — |
| Product | HCID 15636997 | HCID 15636997 | 97% |
Reaction Steps
1,3-Dihydro-5-methyl-6-phenyl-2H-imidazo[4,5-b]pyridin-2-one (Example 4c, 8.06 g) was added in small portions to 80 ml 90% nitric acid cooled to -2° C. The reaction mixture was stirred at 0° C. for 2 hours and then poured portionwise into ice-water. The solid product was collected, washed with water and ether, and dried in high vacuum at 110°-130° C. to give 9.3 g (97%) of 1,3-dihydro-5-methyl-6-(4-nitrophenyl)-2H-imidazo[4,5-b]pyridin-2-one, m.p. above 300° C. Further purification was accomplished by repeated recrystallization from aqueous dimethylformamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05010086 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-31693d9ff9af4ae1a56cb6a7d866c18f |
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| Source note | uspto-grants-1991_04 |
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