HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 6-Aminobenzothieno[3,2-h]Isoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 6-Carbethoxyaminobenzothieno[3,2-h]isoquinoline | HCID 301211 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Aminobenzothieno[3,2-h]Isoquinoline | HCID 301923 | 103% |
Reaction Steps
Two hundred mg (0.62 mM) of 6-carbethoxyaminobenzothieno[3,2-h]isoquinoline (9), prepared in the preceding Example, was added to a solution of 2 g KOH in 5 ml ethanol and 2 ml water. Two layers formed. The mixture was stirred and heated at reflux for approximately 2-3 hr. A yellow solid separated after about an hour, and was collected via filtration and air dried to give 160 mg product, m.p. 220° C.-225° C. This initial product was recrystallized twice from a mixture of DMF and water to provide 120 mg final product, m.p. 223.5° C.-224.5° C., which was then characterized via I.R. and mass spectrometry as compound 10.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05424315 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-dfe888c2a2ea4c15bdff73fa9e7ebe00 |
| Source note | uspto-grants-1995_06 |