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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567703Generated: November 3, 2026

Pyridine → 4-Chloro-5,6,7,8-tetrahydrocinnoline-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/567703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantLithium ChlorideHCID 433294—
Reactant4-Oxo-1,4,5,6,7,8-hexahydrocinnoline-3-carboxylic acid ethyl esterHCID 54107858—
SolventDichloromethaneHCID 6344—
Product4-Chloro-5,6,7,8-tetrahydrocinnoline-3-carboxylic acid ethyl esterHCID 5389717161%

Reaction Steps

To a slurry of 4-oxo-1,4,5,6,7,8-hexahydrocinnoline-3-carboxylic acid ethyl ester (1 g), lithium chloride (0.19 g) and pyridine (0.36 ml) in dichloromethane (30 ml) was added p-toluenesulphonyl chloride (0.85 g). The reaction mixture was heated at reflux for 20 h. The solid was collected by filtration, and the filtrate was evaporated under reduced pressure. The residue was purified by flash chromatography using a gradient elution: CH2Cl2 (500 ml), CH2Cl2/MeOH 99:1 (500 ml), CH2Cl2/MeOH 98:2 (1 liter). The appropriate fractions were combined and evaporated under reduced pressure to give a solid (0.65 g, 61%). δH (360 MHz; CDCl3) 1.44 (3H, t, J=7 Hz, CH3), 1.89 (4H, m, CH2), 2.85 (2H, t, J=5.7 Hz, CH2), 2.62 (2H, t, J=5.7 Hz, CH2), 4.51 (2H, t, J=7 Hz, CH2), m/z (ESP+) 241/243 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06180630B2
Source datasetuspto-grants-2001_01
ORD IDord-5ee0ebb9e7144e0ab1c7d1276273d512
Source noteuspto-grants-2001_01