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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | 4-Oxo-1,4,5,6,7,8-hexahydrocinnoline-3-carboxylic acid ethyl ester | HCID 54107858 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Chloro-5,6,7,8-tetrahydrocinnoline-3-carboxylic acid ethyl ester | HCID 53897171 | 61% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06180630B2 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-5ee0ebb9e7144e0ab1c7d1276273d512 |
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| Source note | uspto-grants-2001_01 |
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