HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 1,4-Dichloroisoquinoline-7-sulfonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 4-Chloro-1-hydroxy-7-isoquinolinesulfonyl chloride | HCID 16658351 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1,4-Dichloroisoquinoline-7-sulfonyl chloride | HCID 16658294 | 84.2% |
Reaction Steps
Phosphorus oxychloride (POCl3) (9.65 mL, 103.5 mmol) was added to a stirred suspension of 4-chloro-7-chlorosulphonyl-1-(2H)-isoquinolone (22.1 g, 79.6 mmol) in MeCN (500 mL) at room temperature and the mixture was then heated at reflux for 15 h. On cooling, the MeCN solution was decanted from the insoluble sludge and evaporated in vacuo. The residue was extracted with hot EtOAc and evaporated to leave a solid which was stirred with Et2O (1.2 L) at room temperature overnight. The ethereal solution was decanted from the insoluble material and evaporated in vacuo to give 7-chlorosulphonyl-1,4-dichloroisoquinoline (20 g, 67 mmol) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06248738B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-c24f4ee4e02941e2b8badf179b698531 |
| Source note | uspto-grants-2001_06 |