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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099372Generated: October 30, 2026

Methoxyacetic Acid → HCID 11612589, compound

https://huagongshe.com/reaction/2099372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethoxyacetic AcidHCID 12251—
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—
ReactantHCID 67415388HCID 67415388—
SolventDichloromethaneHCID 6344—
ProductHCID 11612589HCID 1161258980.1%

Reaction Steps

HATU (0.24 g) was added to a solution of N-(3-chloro-2-fluorophenyl)-6-methoxy-7-(piperidin-4-yloxy)quinazolin-4-amine dihydrochloride (250 mg), diisopropylethylamine (0.37 ml) and methoxyacetic acid (0.054 g) in methylene chloride (9 ml) and the mixture was stirred at room temperature for 2.5 hours. Methylene chloride (20 ml) was added and the organic layer was washed with aqueous sodium hydroxide (2M, 30 ml) and water (30 ml). The resulting product was purified by flash column chromatography eluting with methanol (3%) and methylene chloride (97%) to give a foam. This was re-precipitated by stirring in diethyl ether (20 ml) to give the title product as a white solid (0.200 g); 1H N Spectrum: (DMSO d6 373K) 1.73 (m, 2H), 2.02 (m, 2H), 3.37 (s, 3H), 3.41 (m, 2H), 3.77 (m, 2H), 3.98 (s, 3H), 4.09 (s, 2H), 4.85 (m, 1H), 7.26 (m, 1H), 7.30 (s, 1H), 7.39 (m, 1H), 7.59 (m, 1H), 7.81 (s, 1H), 8.38 (s, 1H), 9.34 (br s, 1H); Mass Spectrum: (M+H)+ 475.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569577B2
Source datasetuspto-grants-2009_08
ORD IDord-e480d83f307d4033a152a4189eb8d05e
Source noteuspto-grants-2009_08