Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 22674120 | HCID 22674120 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 22674044 | HCID 22674044 | — |
Reaction Steps
In dimethyl sulfoxide (1 ml) was dissolved 57 mg of 1-chloro-6-(4-chlorobenzenesulfonylamino)isoquinoline (Example 61). To the mixture were added ethanol (0.1 ml) and 60% sodium hydride (14 mg), followed by heating under stirring at 80° C. for 9 hours. After standing to cool, water was added thereto and the mixture was extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate and the solvent was evaporated. Then, the residue was purified by preparative TLC and solidified from isopropyl ether, to give the title compound (21 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06787534B2 |
|---|
| Source dataset | uspto-grants-2004_09 |
|---|
| ORD ID | ord-594c00821b184c0fbbbe924a54f231d0 |
|---|
| Source note | uspto-grants-2004_09 |
|---|