HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-(7-Bromo-3-isoquinolinyl)ethyl 4-methylbenzenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(7-Bromo-3-isoquinolinyl)ethanol | HCID 21043927 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(7-Bromo-3-isoquinolinyl)ethyl 4-methylbenzenesulfonate | HCID 86592226 | — |
Reaction Steps
The product from Example 52E (0.51 g, 2.0 mmol), tosyl chloride (0.68 g, 3.6 mmol), triethylamine (0.55 g, 5.4 mmol), and DMAP (25 mg, 0.2 mmol) were combined in dichloromethane (20 mL) and stirred at room temperature for 6 hours. The mixture was treated with water (0.5 mL), stirred for 2 hours, and then treated with additional water (15 mL). The organic layer was separated, washed with aqueous sodium chloride solution (10 mL, 10%), evaporated in vacuo, and the residue was azeotroped with heptane (15 mL) to provide the title compound which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07947711B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-43575af23dca42359c81398e9d04f98f |
| Source note | uspto-grants-2011_05 |