HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → (+/-)-1-(2-Mercapto-1-oxopropyl)-1,2,3,4-tetrahydro-2-quinolinecarboxylic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 2-Quinolinecarboxylic acid,1-[2-(benzoylthio)-1-oxopropyl]-1,2,3,4-tetrahydro- | HCID 13336761 | — |
| Solvent | Water | HCID 962 | — |
| Product | (+/-)-1-(2-Mercapto-1-oxopropyl)-1,2,3,4-tetrahydro-2-quinolinecarboxylic Acid | HCID 13336762 | — |
Reaction Steps
(±)-1-(2-Benzoylthio-1-oxopropyl)-1,2,3,4-tetrahydro-2-quinolinecarboxylic acid (4.5 g), concentrated ammonium hydroxide (8 ml) and water (16 ml) were combined and stirred at room temperature under nitrogen for three hours. The benzamide was filtered and the filtrate diluted with water (25 ml). The reaction mixture was then extracted with ethyl acetate and acidified with concentrated hydrochloric acid. The product was extracted with chloroform and the chloroform extracts dried over sodium sulfate and activated charcoal, and concentrated in vacuo. The residue, (±)-1-(2-mercapto-1-oxopropyl)-1,2,3,4-tetrahydro-2-quinolinecarboxylic acid, was triturated with carbon tetrachloride (20 ml); yield 3.2 g, m.p. 141°-143°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04461896 |
| Source dataset | uspto-grants-1984_07 |
| ORD ID | ord-b933a63afc164801be42eed3a391cf2c |
| Source note | uspto-grants-1984_07 |