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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169276Generated: October 26, 2026

Dimethylformamide dimethyl acetal → HCID 54073013, compound

https://huagongshe.com/reaction/1169276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamide dimethyl acetalHCID 78373—
Reactant6-fluoro-2-methyl-3-(2-methyl-pyridin-3-yl)-3H-quinazolin-4-oneHCID 22347424—
SolventDimethylformamideHCID 6228—
ProductHCID 54073013HCID 5407301356.1%

Reaction Conditions

Temperature140 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06627755B1
Source datasetuspto-grants-2003_09
ORD IDord-160dcae0f2b04b0abfad6e7662816434
Source noteuspto-grants-2003_09