HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462710Generated: October 30, 2026
Formamidine acetate → 5-methyl-2-oxo-1H-1,6-naphthyridine-3-carbonitrile
https://huagongshe.com/reaction/462710
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formamidine acetate | HCID 160693 | — |
| Reactant | HCID 53841137 | HCID 53841137 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-methyl-2-oxo-1H-1,6-naphthyridine-3-carbonitrile | HCID 5713068 | 103.1% |
Reaction Steps
E-1. 1,2-Dihydro-5-methvl-2-oxo-1,6-naphthyridine-3-carbonitrile--A mixture containing 33.2 g of 5-acetyl-1,2-dihydro-6-(2-dimethylaminoethenyl)-2-oxo-3-pyridincarbonitrile, 32.1 g of formamidine acetate and 300 ml of dimethylformamide was heated in a oil bath at 120°-130° C. for 3 hours, the original yellow solid dissolving and dark solution resulting. The reaction mixture was evaporated to dryness and then treated with 400 ml of water followed by 30 ml of acetic acid. The resulting insoluble solid was collected, washed with water, air-dried, recrystallized from dimethylformamide and dried at 90° C. to yield 27.4 g of 1,2-dihydro-5-methyl-2-oxo-1,6-naphthyridine-3-carbonitrile as a compound containing 1/2 mole of dimethylformamide, m.p. 278°-280° C. with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04517190 |
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| Source dataset | uspto-grants-1985_05 |
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| ORD ID | ord-1a1c203ab9f4465a9e7a734f7bd59abf |
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| Source note | uspto-grants-1985_05 |
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