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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462915Generated: November 1, 2026

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

https://huagongshe.com/reaction/1462915

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Quinolinecarboxylic acid,1-[2-(benzoylthio)-1-oxopropyl]-1,2,3,4-tetrahydro-HCID 13336761—
Reactant2-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 acidHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04461896
Source datasetuspto-grants-1984_07
ORD IDord-6f0de99cf5d14122904eb3b80234d42b
Source noteuspto-grants-1984_07