HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271549Generated: October 26, 2026
Hydrochloric Acid → HCID 178519793, compound
https://huagongshe.com/reaction/2271549
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (6-Bromo-4-chloroquinolin-3-yl)(cyclopropyl)methanone | HCID 66715111 | — |
| Reactant | HCID 178453933 | HCID 178453933 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178519793 | HCID 178519793 | 52.4% |
Reaction Steps
To a solution of tert-butyl (trans-4-(((R)-3-fluoropyrrolidin-1-yl)methyl)cyclohexyl)carbamate (265 mg, 0.88 mmol) in THF (6 mL) was added aqueous 6N HCl (6 mL) and water (6 mL) and the reaction mixture was heated at 65° C. for 3 h. The reaction mixture was cooled to room temperature, diluted with satd. aq. sodium bicarbonate (50 mL) and 1 M aqueous sodium hydroxide (50 mL) and extracted with a mixture of CHCl3/isopropanol (3:1). The combined organic layers were dried over anhydrous sodium sulfate and concentrated to afford a white semisolid. The residue was dissolved in dioxane followed by the addition of (6-bromo-4-chloroquinolin-3-yl)(cyclopropyl)methanone (225 mg, 0.724 mmol), K2CO3 (415 mg, 3.0 mmol), and N,N-diisopropylethylamine (0.39 mL, 3.0 mmol) and the resultant suspension was heated at 80° C. for 16 h. The reaction was cooled to room temperature, diluted with satd. aq. NaHCO3 and extracted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and concentrated. Purification by column chromatography (silica, 0-20% methanol/dichloromethane) afforded the desired product (180 mg, 52%) as an off-white solid. ESI MS m/z 474 [C24H29BrFN3O+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09120749B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-01e23f7982df48a0a4ba51a00903d841 |
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| Source note | uspto-grants-2015_09 |
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