HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiazole → Thiourea, N-ethyl-N'-2-thiazolyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ethyl isothiocyanate | HCID 10966 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Thiourea, N-ethyl-N'-2-thiazolyl- | HCID 4762507 | 13% |
Reaction Steps
A solution of ethyl isothiocyanate (1.74 g, 20 mmol) and 2-aminothiazole (2.0 g, 20 mmol) in N,N-dimethylformamide (50 mL) was heated at 100° C. for 23 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 twice from ethyl acetate to provide 0.48 g (13%) 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-d1aa0f1a5ed244b98b66ba699e7fc273 |
| Source note | uspto-grants-1997_01 |