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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548696Generated: October 26, 2026

Water → 3-[(8-chloro-2,3-dimethyl-4-oxo-3,4-dihydro-2h-1,3-benzoxazin-7-yl)oxy]-5-{[(1S)-1-(hydroxymethyl)propyl]oxy}-n-(1-methyl-1h-pyrazol-3-yl)benzamide

https://huagongshe.com/reaction/548696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantN-(2-{[tert-Butyl(dimethyl)silyl]oxy}ethyl)-3-chloro-2,4-difluoro-N-methylbenzamideHCID 57663164—
Reactant3-hydroxy-5-{[(1S)-1-(hydroxymethyl)propyl]oxy}-N-(1-methyl-1H-pyrazol-3-yl)benzamideHCID 59127149—
SolventDimethylacetamideHCID 31374—
Product3-[(8-chloro-2,3-dimethyl-4-oxo-3,4-dihydro-2h-1,3-benzoxazin-7-yl)oxy]-5-{[(1S)-1-(hydroxymethyl)propyl]oxy}-n-(1-methyl-1h-pyrazol-3-yl)benzamideHCID 15949496159.5%

Reaction Steps

A solution of 3-hydroxy-5-{[(1S)-1-(hydroxymethyl)propyl]oxy}-N-(1-methyl-1H-pyrazol-3-yl)benzamide (200 mg, 0.66 mmol), N-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-3-chloro-2,4-difluoro-N-methylbenzamide (239 mg, 0.66 mmol) and potassium carbonate (181 mg, 1.31 mmol) in DMA (3 mL) was heated in a microwave reactor at 160° C. for 6 hours. Water (20 mL) was added and the reaction mixture extracted with ethyl acetate. The organic layer was washed with brine (20 mL), dried (MgSO4) and evaporated to a residue which was chromatographed on silica, eluting with 2% methanol in ethyl acetate, and then chromatographed by preparative HPLC on C18 reversed phase, eluting with 5-95% acetonitrile (+0.2% TFA) in water (+0.2% TFA), to give the required product (542 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943607B2
Source datasetuspto-grants-2011_05
ORD IDord-140cbb0bf8274483a33c587fb88554d2
Source noteuspto-grants-2011_05