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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532100Generated: November 1, 2026

Imidazole → 5-[2-Ethoxy-5-(1-imidazolyl)phenyl]-1-methyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]-pyrimidin-7-one

https://huagongshe.com/reaction/1532100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantPotassium CarbonateHCID 11430—
Reactant5-(5-Bromo-2-ethoxyphenyl)-1-methyl-3-propyl-1H-pyrazolo[4,3-D]pyrimidin-7(6H)-oneHCID 135738554—
CatalystCopperHCID 23978—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-[2-Ethoxy-5-(1-imidazolyl)phenyl]-1-methyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]-pyrimidin-7-oneHCID 13573857277.2%

Reaction Steps

A solution of 5-(5-bromo-2-ethoxyphenyl)-1-methyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one (0.20 g, 0.00051 mol), imidazole (0.172 g, 0.00025 mol), anhydrous potassium carbonate (0.077 g, 0.00056 mol), copper bronze (0.036 g, 0.00057 mol) and iodine (0.015 g, 0.00012 mol) in dimethylformamide (10 ml) was heated under reflux under nitrogen for 4.5 hours, cooled and poured into water (50 ml). This mixture was extracted with a 9:1 mixture of dichloromethane and methanol (6×50 ml) and the extracts combined, dried (MgSO4) and evaporated under vacuum to give a pale brown oil. The oil was chromatographed on silica gel (20 g), eluting with a mixture of dichloromethane, methanol and triethylamine (97.8:2:0.2), to give a yellow solid, crystallization of which from ethyl acetate-hexane gave the title compound as a cream solid (0.073 g, 38%), mp. 193-194° C. Found: C, 63.61; H,5.97; N,22.03. C20H22N8O2 requires C,63.48; H,5.86; N,22.21%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06200980B1
Source datasetuspto-grants-2001_03
ORD IDord-84f9aa918e834571bff8dc89ef44f452
Source noteuspto-grants-2001_03