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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175069Generated: October 26, 2026

3,5-Dimethylisoxazole-4-carboxylic acid → HCID 11386930, compound

https://huagongshe.com/reaction/1175069

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dimethylisoxazole-4-carboxylic acidHCID 75636—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant4-(3-Chloro-2-fluoroanilino)-7-methoxy-6-(piperidin-4-yloxy)quinazoline dihydrochlorideHCID 57476865—
SolventDichloromethaneHCID 6344—
ProductHCID 11386930HCID 1138693032.3%

Reaction Steps

HATU (0.31 g) was added to a solution of N-(3-chloro-2-fluorophenyl)-7-methoxy-6-(piperidin-4-yloxy)quinazolin-4-amine dihydrochloride (300 mg), diisopropylethylamine (0.45 ml) and 3,5-dimethyl-4-isoxazolecarboxylic acid (0.141 g) in methylene chloride (9 ml). The resulting mixture was stirred at room temperature for 2.5 hrs. Methylene chloride (20 ml) was added and the organics washed with aqueous sodium hydroxide (2M, 30 ml) and water (30 ml). The crudes were then purified by flash column chromatography eluting with methanol/methylene chloride (2.5/97.5). Fractions containing the desired product were evaporated to a white foam which was triturated with diethyl ether (20 ml) to give N-(3-chloro-2-fluorophenyl)-6-({1-[(3,5-dimethylisoxazol-4-yl)carbonyl]piperidin-4-yl}oxy)-7-methoxyquinazolin-4-amine as a white solid (0.107 g). 1H NMR Spectrum: (DMSO d6 373K) 1.80 (m, 2H), 2.01 (m, 2H), 2.20 (s, 3H), 2.40 (s, 3H), 3.47 (m, 2H), 3.75 (m, 2H), 3.96 (s, 3H), 4.76 (m, 1H), 7.23 (m, 1H), 7.23 (s, 1H), 7.40 (m, 1H), 7.58 (m, 1H), 7.89 (s, 1H), 8.39 (s, 1H), 9.25 (br s, 1H); Mass Spectrum: (M+H)+ 526.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838530B2
Source datasetuspto-grants-2010_11
ORD IDord-4dfed4e90225498e983bfa4dabe85008
Source noteuspto-grants-2010_11