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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485534Generated: October 31, 2026

4-Amino-3,5-dimethylisoxazole → 6-chloro-N-(3,5-dimethyl-4-isoxazolyl)-Pyrido[3,2-d]pyrimidin-4-amine

https://huagongshe.com/reaction/1485534

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-3,5-dimethylisoxazoleHCID 182040—
ReactantSodium AcetateHCID 517045—
Reactant6-chloro-4-[(tetrahydro-2H-pyran-4-yl)oxy]-Pyrido[3,2-d]pyrimidineHCID 86671065—
SolventEthyl AcetateHCID 8857—
Product6-chloro-N-(3,5-dimethyl-4-isoxazolyl)-Pyrido[3,2-d]pyrimidin-4-amineHCID 8667107659.5%

Reaction Steps

A mixture of 4,6-dichloropyrido[3,2-d]pyrimidine (Intermediate 1, step D) (0.100 g, 0.500 mmol), 3,5-dimethylisoxazol-4-amine (0.140 g, 1.250 mmol) and sodium acetate (0.123 g, 1.50 mmol) in 5 ml of solvent (THF:H2O=1:1) was refluxed for 1 hour. The reaction mixture was diluted with EtOAc. The organics were washed with brine, dried over Na2SO4, filtered and concentrated. The crued was purified by column chromatography on SiO2 (Hex:EtOAc=1:1) to get N-(6-chloropyrido[3,2-d]pyrimidin-4-yl)-3,5-dimethylisoxazol-4-amine (0.082 g, 59%) as a yellow solid. 1H-NMR (CDCl3, Varian 400 MHz) δ 2.24 (3H, s), 2.40 (3H, s), 7.74 (1H, d, J=8.8 Hz), 7.93 (1H, brs), 8.16 ((1H, d, J=8.8 Hz), 8.69 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422298B2
Source datasetuspto-grants-2016_08
ORD IDord-b0f8cf78b42040d4a2750776017f1fe9
Source noteuspto-grants-2016_08