HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855840Generated: October 31, 2026
4-(((2-Aminoethyl)thio)methyl)-5-methylimidazole → HCID 3054539, compound
https://huagongshe.com/reaction/1855840
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(((2-Aminoethyl)thio)methyl)-5-methylimidazole | HCID 665568 | — |
| Reactant | HCID 14338588 | HCID 14338588 | — |
| Product | HCID 3054539 | HCID 3054539 | — |
Reaction Steps
An intimate mixture of 5-(2-thienylmethyl)-2-methylthio-4-pyrimidone (1.43 g) and 2-(5-methyl-4-imidazolylmethylthio)ethylamine (1.03 g) was heated at 140° for 6 hours. The cooled residue was washed with water to give 2-[2-(5-methyl-4-imidazolylmethylthio)ethylamino]-5-(2-thienylmethyl)-4-pyrimidone, and this product was treated with dilute ethanolic HCl to give the title compound in 40% yield, m.p. 172°-176° (ethanol-acetonitrile). The dihydrochloride was passed down an ion-exchange column of IRA 400 eluting with 1 N hydrobromic acid, and the eluate was evaporated to dryness and recrystallised from ethanol acetonitrile to give the corresponding dihydrobromide m.p. 99°-203°. (Found: C, 36.7; H, 4.2; N, 13.5; S, 12.1; Br, 30.6; C16H19N5OS2.2HBr Requires: C, 36.7; H, 4.0; N, 13.4; S, 12.2; Br, 30.5%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04216318 |
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| Source dataset | uspto-grants-1980_08 |
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| ORD ID | ord-68f1443195034cf394a52a56ad2544b4 |
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| Source note | uspto-grants-1980_08 |
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