HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169276Generated: October 26, 2026
Dimethylformamide dimethyl acetal → HCID 54073013, compound
https://huagongshe.com/reaction/1169276
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | 6-fluoro-2-methyl-3-(2-methyl-pyridin-3-yl)-3H-quinazolin-4-one | HCID 22347424 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54073013 | HCID 54073013 | 56.1% |
Reaction Steps
A mixture of 6-fluoro-3,4-dihydro-2-methyl-3-(2-methyl-pyridin-3-yl)-quinazolin-4-one (1.02 g, 3.79 mmol) and dimethylformamide dimethyl acetal (1.01 mL, 7.58 mmol) in dimethylformamide (5 mL) was heated to 140° C. for 24 hours. Additional dimethylformamide dimethyl acetal (2 mL) was added and the reaction was heated at 140° C. for 16 hours. The reaction was cooled to ambient temperature and concentrated at reduced pressure. The dark residue was triturated with ether and the dark purple crystalline solid which formed was collected and dried to give 0.69 g (56%) of 6-fluoro-2-(2-dimethylamino-vinyl)-3,4-dihydro-3-(2-methyl-pyridin-3-yl)-quinazolin-4-one which had: 1H NMR δ 8.61 (dd, J=1.5, 5 Hz, 1H), 7.87 (d, J=12.3 Hz, 1H), 7.78 (dd, J=3, 8.5 Hz, 1H), 7.50-7.45 (m, 2H), 7.39-7.29 (m, 2H), 3.97 (d, J=12.3 Hz, 1H), 2.86 (br s, 6H), 2.35 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06627755B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-160dcae0f2b04b0abfad6e7662816434 |
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| Source note | uspto-grants-2003_09 |
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