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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502046Generated: November 3, 2026

Sodium Methoxide → HCID 22636109, compound

https://huagongshe.com/reaction/502046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 22636119HCID 22636119—
SolventMethanolHCID 887—
ProductHCID 22636109HCID 2263610976.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium methoxide (95%, 0.26 g) was added to a stirred solution of 3-(3-acetoxybenzamido)-4-chloro-N-(3-fluoro-5-morpholinophenyl)benzamide (1.23 g) in methanol (75 ml) which had been cooled to 0° C. The resultant solution was stirred at ambient temperature for three hours. The mixture was concentrated by evaporation to a volume of about 15 ml and water (20 ml) was added. The solution was acidified to pH3 by the addition of 1N aqueous hydrochloric acid solution. The precipitate so formed was isolated and dried under vacuum. There was thus obtained the title compound (0.86 g); NMR Spectrum: (DMSOd6) 2.47 (s, 3H), 3.08 (t, 4H), 3.7 (t, 4H), 6.53 (d, 1H), 6.98 (m, 1H), 7.14 (s, 1H), 7.19 (d, 1H), 7.33 (m, 1H), 7.42 (d, 1H), 7.70 (d, 1H), 7.84 (m, 1H), 8.15 (d, 1H), 9.75 (s, 1H), 10.08 (s, 1H), 10.29 (s, 1H); Mass Spectrum: M+H+ 470.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772432B2
Source datasetuspto-grants-2010_08
ORD IDord-5e1444212e404b03bccd977e1d795610
Source noteuspto-grants-2010_08