Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrous Acid | HCID 24529 | — |
| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Reactant | 8-Isoquinolinamine,7-chloro-(9CI) | HCID 21393843 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Product | HCID 21393854 | HCID 21393854 | — |
Reaction Steps
8-Amino-7-chloroisoquinoline (0.005 mole), prepared as in Example 12, in 40% fluoboric acid (30 ml.) is cooled to -10° C. and diazotized with finely powdered sodium nitrite (3.5 g.). After 30 minutes, the reaction mixture is tested for nitrous acid with starch/iodide paper as described in Example 15. When a positive reaction is obtained, the reaction mixture is washed with small portions of ether and then agitated with a mixture of ethanol and ether (20 ml. each). The diazonium tetrafluoroborate is filtered, washed with ether, dried in vacuo and decomposed on an oil bath at approximately 150° C. The residue is partitioned between ether and 5% aqueous sodium hydroxide solution. The ether phase and extracts are combined, washed with water, dried over sodium sulfate and evaporated to yield 7-chloro-8-fluoroisoquinoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04062961 |
|---|
| Source dataset | uspto-grants-1977_12 |
|---|
| ORD ID | ord-281825ef306a41538fa1a16d1bad68f0 |
|---|
| Source note | uspto-grants-1977_12 |
|---|