HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 18925359, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | [1]Benzothiolo[3,2-h]isoquinoline-6-carbonitrile | HCID 304619 | — |
| Solvent | Glycerol | HCID 753 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 18925359 | HCID 18925359 | — |
Reaction Steps
One hundred thirty mg (0.5 mM) of 6-cyanobenzothieno[3,2-h]isoquinoline (4), prepared in Example 1, was suspended in a hot solution of 168 mg (3 mM) KOH in 1 ml glycerine. The reaction mixture was stirred and heated at 160° C.-170° C. overnight. The resulting yellow solution was cooled, diluted with water and made slightly acidic with glacial acetic acid. A yellow precipitate was collected, washed with water, and air dried to yield 120 mg of product. This initial product was recrystallized from a mixture of DMSO and water to give 78 mg product, mp greater than about 305° C. This then was dried at 80° C./0.2 mm overnight, and characterized as compound 6 using I.R. and mass spectrometry.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05424315 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-5c250430b529499aa12d2ccbd03a77bb |
| Source note | uspto-grants-1995_06 |