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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158261Generated: October 30, 2026

Hydrogen Peroxide → HCID 11515891, compound

https://huagongshe.com/reaction/1158261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 11551796HCID 11551796—
SolventAcetic AcidHCID 176—
ProductHCID 11515891HCID 11515891—

Reaction Steps

To a stirred solution of (4-Chloro-phenyl)-[2-(3-dimethylamino-propylsulfanyl)-3-methyl-3H-imidazol-4-yl]-methanone (135 mg) in glacial acetic acid (4.00 mL) was added at rt H2O2 (82.0 μL; 30 wt. % in water). The reaction solution was stirred for 48 h at rt, and water (10.0 mL) was added. The solution was brought to pH=12 using NaOH (25% in water) and extracted with CH2Cl2 (250 mL, 2×50.0 mL). The combined organic layers were washed with water (3×20.0 mL) and were dried over MgSO4. The solvent was removed in vacuo, and the residue was purified by flash chromatography on silica gel (CHCl3/2 M NH3 in MeOH) to give the title compound (121 mg). M calc=353; M+H found=354; 1H NMR (400 MHz, CD3OD): δ 7.91-7.87 (m, 2H), 7.70 (s, 1H), 7.60-7.55 (m, 2H), 4.21 (s, 3H), 3.61-3.48 (m, 2H), 2.54-2.43 (m, 2H), 2.21 (s, 6H), 2.04-1.94 (m, 2H). The compound demonstrated useful biological activity when assessed with a [3H]-N-methylhistamine binding assay (see Table in Example XXV).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807837B2
Source datasetuspto-grants-2010_10
ORD IDord-5e4a3f7147a543658b50f4b8820ae099
Source noteuspto-grants-2010_10