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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854853Generated: October 29, 2026

O-Methylhydroxylamine hydrochloride → 2-(3-chloro-4-methanesulfonyl-phenyl)-3-(4-methoxyimino-cyclohexyl)-N-pyrazin-2-yl-propionamide

https://huagongshe.com/reaction/854853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
Reactant2-(3-chloro-4-methanesulfonyl-phenyl)-3-(4-oxo-cyclohexyl)-N-pyrazin-2-yl-propionamideHCID 10342959—
SolventMethanolHCID 887—
SolventPyridineHCID 1049—
Product2-(3-chloro-4-methanesulfonyl-phenyl)-3-(4-methoxyimino-cyclohexyl)-N-pyrazin-2-yl-propionamideHCID 2195897681.2%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of methoxylamine hydrochloride (23 mg, 0.27 mmol) in methanol (0.5 mL) and pyridine (0.5 mL) was treated with 2-(3-chloro-4-methanesulfonyl-phenyl)-3-(4-oxo-cyclohexyl)-N-pyrazin-2-yl-propionamide (prepared as in Example 58, 80 mg, 0.18 mmol). The reaction mixture was heated under reflux for 2 h, cooled to 25° C., and concentrated in vacuo to remove methanol. The resulting residue was suspended in ethyl acetate (10 mL), washed with water 1×5 mL), dried over magnesium sulfate, filtered, and concentrated in vacuo. Biotage chromatography (FLASH 12M, Silica, 35/65 hexanes/ethyl acetate) afforded 2-(3-chloro-4-methanesulfonyl-phenyl)-3-(4-methoxyimino-cyclohexyl)-N-pyrazin-2-yl-propionamide (68 mg, 81%) was a white foam: EI-HRMS m/e calcd for C21H25ClN4O4S (M+H)+ 465.1358. found 465.1364.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259166B2
Source datasetuspto-grants-2007_08
ORD IDord-4cbc567837b74ac290a7076acb449abb
Source noteuspto-grants-2007_08