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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494934Generated: October 30, 2026

Sodium Hydroxide → HCID 76591490, compound

https://huagongshe.com/reaction/494934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium AcetateHCID 517045—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
ReactantHCID 57682902HCID 57682902—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
ProductHCID 76591490HCID 7659149067.9%

Reaction Steps

97 mg of 1-(1-(2-(8-methoxy-5-oxo-2,3,4,5-tetrahydrobenzo[b]oxepin-7-yl)ethyl)piperidin-4-yl)-1H-indole-6-carboxamide was dissolved in a mixed solution consisting of 4 ml of methanol, 2 ml of tetrahydrofuran, and 2 ml of chloroform. Thereafter, 105 mg of methoxylamine hydrochloride and 103 mg of sodium acetate were added to the reaction solution, and the obtained mixture was then stirred at room temperature. At the midpoint of the reaction, 1 g of methoxylamine hydrochloride and 1 g of sodium acetate were further added thereto. After completion of the reaction, a 1 N sodium hydroxide aqueous solution, a saturated sodium bicarbonate aqueous solution, and chloroform were added to the reaction solution, so as to separate an organic layer. The obtained organic layer was washed with a saturated sodium bicarbonate aqueous solution and a saturated sodium chloride solution, and then dried over anhydrous magnesium sulfate. After removing the drying agent by filtration, the organic layer was concentrated under a reduced pressure. The residue was solidified from t-butyl methyl ether-ethyl acetate, so as to obtain 70 mg of the subject compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538123B2
Source datasetuspto-grants-2009_05
ORD IDord-2ba4a6f25dd040d390eb6c264e966267
Source noteuspto-grants-2009_05