HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5-(2-(Methanesulfonyloxy)ethoxy)-2-methylquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 17965146 | HCID 17965146 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(2-(Methanesulfonyloxy)ethoxy)-2-methylquinazoline | HCID 17965139 | 99% |
Reaction Steps
To a solution of 2-(2-methylquinazolin-5-yloxy)ethanol (0.330 g, 1.62 mmol) in dichloromethane (20 mL) and triethylamine (0.34 mL, 2.43 mmol) was added methane sulfonyl chloride (0.14 mL, 1.78 mmol) dropwise. The reaction mixture was allowed to stir at room temperature for 2 h. The reaction mixture was diluted with further dichloromethane and partitioned with saturated NaHCO3 aq. The organic phase was washed with brine, dried (MgSO4) and evaporated in vacuo to give the title compound as a cream solid (0.452 g, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07214674B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-67a60fbbd19a4a8faa04c4f341ee8969 |
| Source note | uspto-grants-2007_05 |