HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895384Generated: October 30, 2026
2-Aminothiazole → HCID 178478541, compound
https://huagongshe.com/reaction/895384
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Benzhydrylamine | HCID 7036 | — |
| Reactant | Thiocarbonyl diimidazole | HCID 11412697 | — |
| Reactant | HCID 13606189 | HCID 13606189 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178478541 | HCID 178478541 | — |
Reaction Steps
To a stirred solution of 2-aminothiazole (100 mg) in acetonitrile (3 mL) was added thiocarbonyl dimidazole (180 mg, 1.0 mmol). The mixture was allowed to stir at rt for 2 h and at 65° C. for 5 h, and then 1-(2,4-dichlorophenyl)-2-(imidazol-1-yl)ethylamine (250 mg, 1.0 mmol) was added. This was allowed to stir for 5 h at 65° C. The mixture was cooled to rt, and diphenylmethylamine was added, followed by TEA and mercuric chloride. The suspension was allowed to stir at rt for 3 h and filtered. The filtrate was concentrated and the residue purified by column chromatography (EtOAc, MeOH, NH4OH; 90:10:0.1) to give after conversion to HCT salt, the title compound as a yellow solid (100 mg). MS (ES): m/z 547 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06916813B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-d9f6a5190c164e32b2852318ce145482 |
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| Source note | uspto-grants-2005_07 |
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