HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(4-(5-(m-Tolyl)oxazole-4-carboxamido)-1H-pyrazol-1-yl)ethyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 68283198 | HCID 68283198 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-(5-(m-Tolyl)oxazole-4-carboxamido)-1H-pyrazol-1-yl)ethyl methanesulfonate | HCID 86704219 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To an ice-cooled solution of N-(1-(2-hydroxyethyl)-1H-pyrazol-4-yl)-5-(m-tolyl)oxazole-4-carboxamide (178 mg, 0.57 mmol) in DCM (8 mL), Et3N (0.24 mL, 1.71 mmol) was added. After stirring for 5 min at 0° C., methanesulfonyl chloride (0.11 mL, 1.43 mmol) was added dropwise, and the resulting suspension was stirred at 0° C. for 1 h 15, then quenched with water and extracted with DCM (2×). The combined org. layers were washed with brine, dried (MgSO4) and concentrated in vacuo to obtain the title compound as an oil. LC-MS conditions A: tR=0.90 min, [M+H]+=391.03.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09303023B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-b11722ce31644caa88a06bfb6e94f340 |
| Source note | uspto-grants-2016_04 |