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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477453Generated: October 25, 2026

5-Aminoimidazole-4-carboxamide hydrochloride → 4-(3,4-Dimethoxyphenyl)imidazo[1,5-a]pyrimidine-8-carboxamide

https://huagongshe.com/reaction/477453

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Aminoimidazole-4-carboxamide hydrochlorideHCID 66146—
ReactantSodium BicarbonateHCID 516892—
Reactant(E)-1-(3,4-dimethoxyphenyl)-3-(dimethylamino)-2-propen-1-oneHCID 1481361—
SolventAcetic AcidHCID 176—
Product4-(3,4-Dimethoxyphenyl)imidazo[1,5-a]pyrimidine-8-carboxamideHCID 1467747553.8%

Reaction Steps

A stirred mixture of 15.0 g of 3-dimethylamino-3',4'-dimethoxyacrylophenone (prepared as described in Example 6) and 8.0 g of 4-amino-5-imidazolecarboxamide hydrochloride in 150 ml of glacial acetic acid was heated at reflux for 24 hours. The solvent was evaporated in vacuo to give an oil. The oil solidified on standing at room temperature, and this was treated with 200 ml of saturated sodium bicarbonate solution and then it was filtered to collect the crystals. The material was treated by boiling with 700 ml of ethanol and then was filtered. The solid was recrystallized from methanol-chloroform to give 7.9 g of the desired product, mp 262°-265° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04888345
Source datasetuspto-grants-1989_12
ORD IDord-b478f80c5cbd4adb9a7f78e0589823e6
Source noteuspto-grants-1989_12