HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Tert-butyl 1-(4-(4-chloro-5-(trifluoromethyl)pyrimidin-2-ylamino)phenyl)ethylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4-Dichloro-5-(trifluoromethyl)pyrimidine | HCID 2782774 | — |
| Reactant | tert-butyl N-[1-(4-aminophenyl)ethyl]carbamate | HCID 22569414 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | Tert-butyl 1-(4-(4-chloro-5-(trifluoromethyl)pyrimidin-2-ylamino)phenyl)ethylcarbamate | HCID 76611269 | — |
Reaction Steps
2,4-Dichloro-5-(trifluoromethyl)pyrimidine (1.93 g, 8.89 mmol) was stirred in a 1:1 t-BuOH:DCE mixture (200 mL) at room temperature. A 1.0 M ZnCl2 solution in Et2O (10.2 mL, 10.2 mmol) was added cautiously and the mixture was stirred at room temperature for 20 minutes. A 1:1 t-BuOH:DCE mixture (100 mL) was added followed by tert-butyl (1-(4-aminophenyl)ethyl)carbamate (2.00 g, 8.46 mmol) and Et3N (1.42 mL, 10.2 mmol). The mixture was stirred at room temperature overnight before the volatiles were evaporated in vacuo. EtOH (30 mL) was added, the suspension was sonicated for 1 minute before the solid was filtered, washed with EtOH (10 mL) and dried in vacuo to give the title compound A80 as a cream solid (3.2 g, 91%). LCMS-C: rt 4.88 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238644B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-d8c8a23f7c554cd097d6fd06c5592ac3 |
| Source note | uspto-grants-2016_01 |