HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34814Generated: October 29, 2026
Triethylamine → 2-[4-(2-[2-(2,2,2-Trifluoroethyl)guanidino]thiazol-4-yl)butylamino]benzimidazole
https://huagongshe.com/reaction/34814
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-[2-(2,2,2-Trifluoroethyl)-guanidino]-4-[4-(3-[2-aminophenyl]thioureido)butyl]thiazole | HCID 21298698 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[4-(2-[2-(2,2,2-Trifluoroethyl)guanidino]thiazol-4-yl)butylamino]benzimidazole | HCID 21298802 | — |
Reaction Steps
A mixture of 2-[2-(2,2,2-trifluoroethyl)guanidino]-4-[4-(3-[2-aminophenyl]thioureido)butyl]thiazole (0.45 g.), silver nitrate (0.34 g.) and triethylamine (0.28 ml.) in dimethylformamide (3 ml.) was stirred vigorously at ambient temperature overnight. Hydrogen sulphide gas was then bubbled through the reaction mixture until no more solid precipitated. The reaction mixture was filtered through a pad of diatomaceous earth and the filtrate evaporated to dryness in vacuo. The residue was purified by low pressure liquid chromatography using chloroform/methanol/ammonia, 9:1:0.1 v/v/v as eluant to give 2-[4-(2-[2-(2,2,2-trifluoroethyl)guanidino]thiazol-4-yl)butylamino]benzimidazole which was converted to the hydrogen maleate salt (0.25 g.), m.p. 183°-186°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04762932 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-f88166bd501442acbaa779aa63ee732d |
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| Source note | uspto-grants-1988_08 |
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