HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869162Generated: October 26, 2026
Potassium Carbonate → 3-methoxycarbonyl-1-(7-(trifluoromethyl)quinol-4-yl)-1H-indole
https://huagongshe.com/reaction/1869162
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Chloro-7-(trifluoromethyl)quinoline | HCID 67668 | — |
| Reactant | Methyl indole-3-carboxylate | HCID 589098 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-methoxycarbonyl-1-(7-(trifluoromethyl)quinol-4-yl)-1H-indole | HCID 68970594 | 86.4% |
Reaction Steps
1.04 g (7.5 mmol) of potassium carbonate and 0.695 g (3 mmol) of 4-chloro-7-(trifluoromethyl)quinoline are added to 0.525 g (3 mmol) of 3-methoxycarbonyl-1H-indole in 10 cm3 of dimethylformamide under an argon atmosphere. After stirring at a temperature in the region of 100° C. for 20 hours, the reaction mixture is cooled and diluted with 100 cm3 of ethyl acetate and 100 cm3 of water. The organic phase is separated off by settling and washed with twice 100 cm3 of water and 100 cm3 of saturated aqueous sodium chloride solution and then it is dried over magnesium sulphate, filtered and concentrated to dryness under reduced pressure (2.7 kPa), resulting in an orange-coloured oil. This oil is triturated in 20 cm3 of isopropyl ether and the resulting precipitate is filtered off, giving 0.96 g of 3-methoxycarbonyl-1-(7-(trifluoromethyl)quinol-4-yl)-1H-indole in the form of a yellow powder. Mass spectrum (EI): m/e 370 (M+•), m/e 339.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07638521B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-c58b1b237713470ba35e5fb384018159 |
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| Source note | uspto-grants-2009_12 |
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