HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Dimethylaniline → HCID 22716515, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Isocyanatocarbonyl chloride | HCID 119708 | — |
| Reactant | HCID 22716548 | HCID 22716548 | — |
| Product | HCID 22716515 | HCID 22716515 | 67% |
Reaction Steps
To 2-(2-chlorophenyl)-4-(2-fluorophenyl)-4,5-dihydrothiazole (0.303 g, 1.00 mmol) and N,N-dimethylaniline (0.135 mL, 1.05 mmol) in dichloromethane (2 mL) at 0° C. was added dropwise chlorocarbonyl isocyanate (0.080 mL, 1.0 mmol). The mixture was allowed to warm to room temperature and stirred for 24 hours. The resulting suspension was cooled to 0° C., filtered, and washed with ice-cold 1:1 dichloromethane/ether (2×1 mL) to give the title compound as a white powder (0.251 g, 67%). MS=375.1 ((M+H)+). 1H NMR (TMS/DMSO-D6, 400 MHz): 7.59-7.08 (m, 8H); 6.18 (d, J=7.6 Hz, 1H); 4.05 (dd, J=11.2, 7.6 Hz, 1H); 3.25 (d, J=11.2, 1H); 2.87 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06740656B2 |
| Source dataset | uspto-grants-2004_05 |
| ORD ID | ord-e36f33669d59407ba031e17a4ada9a5a |
| Source note | uspto-grants-2004_05 |