HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268333Generated: October 30, 2026
Dimethylformamide → HCID 14663383, compound
https://huagongshe.com/reaction/268333
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 67794569 | HCID 67794569 | — |
| Reactant | HCID 86733186 | HCID 86733186 | — |
| Reactant | HCID 178418268 | HCID 178418268 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14663383 | HCID 14663383 | — |
Reaction Steps
A 100 ml. flask was charged with 9.0 g. of a mixture of N2 -n-butyl-2,3-pyridine-dicarboxamide and N3 -n-butyl-2,3-pyridine-dicarboxamide suspended in 70 g. dimethylformamide. An 18.0 g. portion of lead tetra-acetate was added, and the reaction mixture stirred at 60° for 2 hours. The reaction mixture was poured into 200 ml. water. The precipitate was filtered from the water, recrystallized from dioxane, and dried at 100°, for about 1 hour. The final yield of 3-n-butyl-pyrido[3,2-d] and 3-n-butyl-pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione amounted to 8.4 g., melting point 200°-210°, and represented 93 percent of theory based on the dicarboxamide starting material. The structure was determined by nuclear magnetic resonance spectroscopy to consist of 78 percent of the [3,2-d]isomer and 22 percent of the [2,3-d]isomer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03947442 |
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| Source dataset | uspto-grants-1976_03 |
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| ORD ID | ord-aa5b8067a5d44b3397bb25f8b91e2f3d |
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| Source note | uspto-grants-1976_03 |
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