HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Isocyanate → N-methyl-N'-(4-(1-(2-fluoro-4-biphenylyl)ethyl)thiazol-2-yl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | 2-Amino-4-(1-(2-fluoro-4-biphenylyl)ethyl)thiazole | HCID 10469982 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-methyl-N'-(4-(1-(2-fluoro-4-biphenylyl)ethyl)thiazol-2-yl)urea | HCID 15676061 | 84% |
Reaction Steps
To 2-amino-4-(1-(2-fluoro-4-biphenylyl)ethyl) thiazole (500 mg, 1.68 mmol) in chloroform (20 ml) was added methylisocyanate (0.10 mg, 1.75 mmol) in chloroform (10 ml) under cooling with ice. After the mixture was stirred, methylisocyanate (0.15 mmol, 2.63 mmol) was added to the mixture, and then the mixture was stirred at room temperature overnight. The mixture was evaporated under reduced pressure to a residue, which was crystallized to afford N-methyl-N'-(4-(1-(2-fluoro-4-biphenylyl)ethyl) thiazol-2-yl)urea (0.499 g, 84% yield) as crystalline material: mp 208.5°-209.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05066666 |
| Source dataset | uspto-grants-1991_11 |
| ORD ID | ord-abe49ba4bdf2418ab4f36bd76dfbf9b6 |
| Source note | uspto-grants-1991_11 |