HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235136Generated: October 25, 2026
Chloride → 2-Chloro-4-[(1,2,3,4-tetrahydro-quinoline-7-carbonyl)-amino]-benzoic acid methyl ester
https://huagongshe.com/reaction/2235136
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloride | HCID 312 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | 2-Chloro-4-[(quinoline-7-carbonyl)-amino]-benzoic acid methyl ester | HCID 68698438 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 2-Chloro-4-[(1,2,3,4-tetrahydro-quinoline-7-carbonyl)-amino]-benzoic acid methyl ester | HCID 68696796 | 30% |
Reaction Steps
Water (1.5 ml), 60% aqueous perchloric acid (0.01 ml) and pentamethylcycloopentadienyliridium(III) chloride dimer) (116 mg, 0.145 mmol, 0.05 equiv.) were added to 2-chloro-4-[(quinoline-7-carbonyl)-amino]-benzoic acid methyl ester (1.42 g, 4.17 mmol) in degassed isopropanol (100 ml) under a nitrogen atmosphere and the mixture was refluxed for 48 hours. The mixture was evaporated to give a tan solid. The solid was purified by flash chromatography (SiO2, 1:9 tert-butyl-methyl ether:dichloromethane to 1:1:8 tert-butyl-methyl ether:methanol:dichloromethane). The fractions were combined to afford 2-chloro-4-[(1,2,3,4-tetrahydro-quinoline-7-carbonyl)-amino]-benzoic acid methyl ester, 0.434 g (30% yield) as a tan solid. LC @215 nm; Rt 1.15: 98%, m/z (ES+): 345 (M+H+.); δH (250 MHz; d6-DMSO) 10.39 (1H, br.s), 8.07 (1H, m), 7.91-7.80 (2H, m), 7.05-6.90 (3H, m), 5.95 (1H, br.s), 3.82 (3H, s), 3.19 (2H, m), 2.70 (2H, m), 1.79 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07713996B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-d975ab8e3d284ef69f5bf9059c67a1e6 |
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| Source note | uspto-grants-2010_05 |
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