HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Quinolinecarboxylic acid,1-[2-(benzoylthio)-1-oxopropyl]-1,2,3,4-tetrahydro- → (+/-)-1,2,3,4-Tetrahydro-1-(3-mercapto-1-oxopropyl)-6-methoxy-2-quinolinecarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Quinolinecarboxylic acid,1-[2-(benzoylthio)-1-oxopropyl]-1,2,3,4-tetrahydro- | HCID 13336761 | — |
| Reactant | 2-Quinolinecarboxylic acid,1-[3-(benzoylthio)-1-oxopropyl]-1,2,3,4-tetrahydro-6-methoxy- | HCID 13336763 | — |
| Product | (+/-)-1,2,3,4-Tetrahydro-1-(3-mercapto-1-oxopropyl)-6-methoxy-2-quinolinecarboxylic acid | HCID 13336764 | — |
Reaction Steps
By substituting (±) 1-(3-benzoylthio-1-oxopropyl)-1,2,3,4-tetrahydro-6-methoxy-2-quinolinecarboxylic acid for the (±) 1-(2-benzoylthio-1-oxopropyl)-1,2,3,4-tetrahydro-2-quinolinecarboxylic acid in the procedure of Example 21, (±)-1,2,3,4-tetrahydro-1-(3-mercapto-1-oxopropyl)-6-methoxy-2-quinolinecarboxylic acid was obtained as an oily residue. The dicyclohexylamine salt was prepared by the addition of dicyclohexylamine to a solution of the free acid in ether. The (±)-1,2,3,4-tetrahydro-1-(3-mercapto-1-oxopropyl)-6-methoxy-2-quinolinecarboxylic acid dicyclohexylamine salt thus obtained was recrystallized from acetonitrile; yield 0.9 g, m.p. 195°-197°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04461896 |
| Source dataset | uspto-grants-1984_07 |
| ORD ID | ord-6f0de99cf5d14122904eb3b80234d42b |
| Source note | uspto-grants-1984_07 |