HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiazole → N,N-Dicyclohexyl-N'-1,3-thiazol-2-yl-2-imidodicarbonic diamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Dicyclohexylamine | HCID 7582 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isocyanatocarbonyl chloride | HCID 119708 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N,N-Dicyclohexyl-N'-1,3-thiazol-2-yl-2-imidodicarbonic diamide | HCID 16046747 | — |
Reaction Steps
Prepared as described in General Procedure 2. To chlorocarbonyl isocyanate (0.2 g) in tetrahydrofuran at −20-0° C. was added dicyclohexylamine (1 equivalent) and triethylamine (0.27 mL). After 20 min 2-aminothiazole (0.2 g) was added and the reaction allowed to warm to room temperature over 3 h and stirred overnight at room temperature. The reaction mixture was partially concentrated. The crude product was then dissolved in tetrahydrofuran and purified by flash chromatography (Eluant 20 dichloromethane:1 methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07999114B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-4e11473f457a47d9a3d4a506a54ae6bd |
| Source note | uspto-grants-2011_08 |