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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989903Generated: November 1, 2026

Methanol → HCID 16040144, compound

https://huagongshe.com/reaction/1989903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTriethylamineHCID 8471—
ReactantTriethylsilaneHCID 12052—
ReactantHCID 53629627HCID 53629627—
Catalystpalladium(II) acetateHCID 167845—
SolventDichloromethaneHCID 6344—
ProductHCID 16040144HCID 1604014445.9%

Reaction Steps

Triethylamine (0.025 mL, 0.18 mmol) then triethylsilane (0.96 mL, 6.03 mmol) were added to palladium (II) acetate (12 mg) in DCM (2 mL) and stirred under argon for 15 mins. 3-{[5-(Azetidin-1-ylsulfonyl)-3-bromopyridin-2-yl]oxy}-5-{[(1S)-1-methyl-2-(methyloxy)ethyl]oxy}-N-(1-methyl-1H-pyrazol-3-yl)benzamide (0.175 g, 0.3 mmol) in DCM (2 mL) was added dropwise and the reaction stirred at RT for 24 hours. Methanol was added, the reaction filtered through celite and the solvent removed in vacuo. Ethyl acetate (30 mL) was added and the mixture washed with water (30 mL), citric acid (30 mL), brine (30 mL), dried (MgSO4), filtered and the solvent removed in vacuo to give a white solid. This was chromatographed on silica, eluting with a gradient of 0-100% ethyl acetate in isohexane, to give the desired compound (69 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642263B2
Source datasetuspto-grants-2010_01
ORD IDord-57de179ae1474b629905468dcad23137
Source noteuspto-grants-2010_01