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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154366Generated: October 27, 2026

Isobutylamine → 7-AMINO-2,3-DIHYDRO-8-(2-METHYLPROPYL)IMIDAZO[1,2-a]PYRIMIDIN-5(8H)-ONE

https://huagongshe.com/reaction/1154366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutylamineHCID 6558—
ReactantEthyl cyanoacetateHCID 7764—
ReactantSodiumHCID 5360545—
Reactant1H-Imidazole, 4,5-dihydro-2-(methylthio)-, hydriodide (1:1)HCID 12221228—
SolventEthanolHCID 702—
Product7-AMINO-2,3-DIHYDRO-8-(2-METHYLPROPYL)IMIDAZO[1,2-a]PYRIMIDIN-5(8H)-ONEHCID 13100554—

Reaction Steps

A mixture of 29.25 g. (0.40 mole) isobutylamine and 48.82 g. (0.20 mole) 2-(methylthio)-2-imidazoline hydroiodide in 250 ml. abs. EtOH were refluxed for 2 hr. The mixture was concentrated in vacuo to a viscous oil, which was dissolved in 100 ml. abs. EtOH and added to a solution of 8.40 g. (0.80 mole) sodium and 22.62 g. (0.20 mole) ethyl cyanoacetate in 1200 ml. abs. EtOH. The mixture was refluxed for 3 hr., then concentrated in vacuo to a viscous oil. Water (400 ml.) was added and a white solid slowly crystallized. The solid was filtered and air-dried to yield 35.43 g. (86%), mp 235°-238° (two crops). Recrystallization from CH3CN gave white crystals, mp 230.5°-232.5° (corr.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04489078
Source datasetuspto-grants-1984_12
ORD IDord-749a190358cd45669c9fa84c49be53d7
Source noteuspto-grants-1984_12