HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiazole → N-(2-[1-cyclohexenyl]ethyl)-N'-[2-thiazolyl]thiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1-(2-Isothiocyanatoethyl)cyclohex-1-ene | HCID 2735881 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(2-[1-cyclohexenyl]ethyl)-N'-[2-thiazolyl]thiourea | HCID 3003028 | 50% |
Reaction Steps
A solution of 2-(1-cyclohexenyl)ethyl isothiocyanate (3.3 g, 20 mmol) and 2-aminothiazole (2.0 g, 20 mmol) in N,N-dimethylformamide (20 mL) was heated at 100° C. for 24 h. The reaction was cooled to room temperature, poured into ethyl acetate, washed with water, 1N aqueous HCl, water, saturated sodium bicarbonate, and brine. The organic layer was concentrated and the residue recrystallized from ethyl acetate to provide 2.66 g (50%) of the title product:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05593993 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-047db68311ae44e488a791778d7b9570 |
| Source note | uspto-grants-1997_01 |