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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30506Generated: October 25, 2026

Bromomethyl 4-methoxyphenyl ketone → 5-Amino-2-(1-[4-methoxyphenylcarbonylmethyl]benzimidazol-2-yl)-pyrazole

https://huagongshe.com/reaction/30506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethyl 4-methoxyphenyl ketoneHCID 4965—
ReactantPotassium CarbonateHCID 11430—
Reactant5-amino-2-(1H-benzimidazol-2-yl)pyrazoleHCID 57464472—
SolventWaterHCID 962—
Product5-Amino-2-(1-[4-methoxyphenylcarbonylmethyl]benzimidazol-2-yl)-pyrazoleHCID 57494334—

Reaction Steps

A suspension of 5-amino-2-(1H-benzimidazol-2-yl)pyrazole (0.10 g, 0.5 mmol), p-methoxyphenacyl bromide (0.204 g, 0.9 mmol) and dry potassium carbonate (0.173 g, 1.25 mmol) is stirred at room temperature for 16 hours. The mixture is diluted with water and the product extracted with ethyl acetate. The product is purified by chromatography on silicagel. M.p. 136-140° C., 1H-NMR (400 MHz, d6-DMSO): 8.04 (d, 2H); 7.58 (m, 2H); 7.28 (m, 3H); 7.11 (d, 2H); 6.84 (s, 2H); 6.26 (s, 2H); 5.39 (d, 1H); 3.87 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423157B2
Source datasetuspto-grants-2008_09
ORD IDord-f8b0f03890c64aedba67ef2fd6510344
Source noteuspto-grants-2008_09