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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277217Generated: October 31, 2026

Ammonium Chloride → HCID 86731283, compound

https://huagongshe.com/reaction/2277217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 86731282HCID 86731282—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86731283HCID 86731283—

Reaction Steps

To a solution of 2-((2-(4-(cyclopropylmethoxy)-3-fluorophenyl)-4,5,6,7-tetrahydro-1,3-benzoxazol-6-yl)oxy)-1-(morpholin-4-yl)ethanone (1.68 g) in THF (25 mL) was added methylmagnesium bromide (1 M THF solution, 5.85 mL). To the reaction mixture was added saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. To the obtained residue in a mixed solvent of THF (10 mL)-methanol (10 mL) was added sodium tetrahydroborate (148 mg), and the mixture was stirred at room temperature for 10 min. To the reaction mixture was added saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (920 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133129B2
Source datasetuspto-grants-2015_09
ORD IDord-3ff8e9ac43fb42db9ec02e49c932ca97
Source noteuspto-grants-2015_09