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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716227Generated: October 25, 2026

2-Chloro-1-(1,2,3,4-tetrahydroquinolin-1-yl)ethan-1-one → 1-(3,4-Dihydro-2H-quinolin-1-yl)-2-(1-methyl-1H-benzoimidazol-2-ylsulfanyl)ethanone

https://huagongshe.com/reaction/1716227

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1-(1,2,3,4-tetrahydroquinolin-1-yl)ethan-1-oneHCID 240137—
ReactantHCID 178481665HCID 178481665—
Product1-(3,4-Dihydro-2H-quinolin-1-yl)-2-(1-methyl-1H-benzoimidazol-2-ylsulfanyl)ethanoneHCID 4068869377%

Reaction Steps

The title compound was synthesized according to General Procedure A using compound 4 as the electrophile and 1-methyl-1H-benzo[d]imidazole-2-thiol as the nucleophile to yield 17 as a pale yellow solid (77%): MS m/z: 338 (M+H)+. Anal. Calcd. For, C19H19N3OS: C, 67.63; H, 5.68; N, 12.45; S, 9.50. Found: C, 67.45; H, 5.74; N, 12.25; S, 9.41.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803790B2
Source datasetuspto-grants-2010_09
ORD IDord-8bb527f3cd9d4d018d6938e6620171eb
Source noteuspto-grants-2010_09