HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826897Generated: November 1, 2026
4-Quinolinecarboxylic acid → HCID 178461350, compound
https://huagongshe.com/reaction/1826897
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Quinolinecarboxylic acid | HCID 10243 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 178461307 | HCID 178461307 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178461350 | HCID 178461350 | 58.1% |
Reaction Steps
A solution of quinoline-4-carboxylic acid (173 mg, 1 mmol), and 1,1′-carbonyldiimidazole (162 mg, 1 mmol) in dimethylformamide (2 mL) was heated at 50° C. for 1 hour. After this time, trans-4-methylcyclohexylamine hydrochloride (150 mg, 1 mmol), and N,N-diisopropylethylamine (0.262 mL, 1.5 mmol) were added and the mixture heated at 50° C. for 16 hours. The reaction mixture was cooled, and diluted with chloroform (10 mL). The organic solution was washed with water (3×10 mL), 1 N NaOH (10 mL), brine (10 mL), dried over anhydrous MgSO4, filtered and concentrated to afford 156 mg (58%) of 403:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07053104B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-efeb5c640ddf4690824c07e8179555ab |
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| Source note | uspto-grants-2006_05 |
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