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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404917Generated: November 1, 2026

2-Chloro-1-(1,2,3,4-tetrahydroquinolin-1-yl)ethan-1-one → 2-(6-Chloro-benzothiazol-2-ylsulfanyl)-1-(3,4-dihydro-2H-quinolin-1-yl)-ethanone

https://huagongshe.com/reaction/1404917

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1-(1,2,3,4-tetrahydroquinolin-1-yl)ethan-1-oneHCID 240137—
ReactantHCID 178527790HCID 178527790—
Product2-(6-Chloro-benzothiazol-2-ylsulfanyl)-1-(3,4-dihydro-2H-quinolin-1-yl)-ethanoneHCID 5946788273%

Reaction Steps

The title compound was synthesized according to General Procedure A using compound 4 as the electrophile and 6-chlorobenzo[d]thiazole-2-thiol as the nucleophile to yield 25 as a white solid (73%): MS m/z: 375 (M+H)+. Anal. Calcd. For, C18H15ClN2OS2: C, 57.67; H, 4.03; N, 7.47; S, 17.11; Cl, 9.46. Found: C, 57.50; H, 4.05; N, 7.48; S, 16.86; Cl, 9.74.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916550B2
Source datasetuspto-grants-2014_12
ORD IDord-224d2c8292e84ea9a28deac22726cc09
Source noteuspto-grants-2014_12