HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192603Generated: October 31, 2026
Tetrahydrofuran → 1-[5-Chloro-8-(3-fluoropiperidin-1-yl)quinolin-7-yl]ethanamine
https://huagongshe.com/reaction/1192603
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 1-[5-Chloro-8-(3-fluoropiperidin-1-yl)quinolin-7-yl]ethanone | HCID 58368489 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-[5-Chloro-8-(3-fluoropiperidin-1-yl)quinolin-7-yl]ethanamine | HCID 58368668 | — |
Reaction Steps
A mixture of 1-[5-chloro-8-(3-fluoropiperidin-1-yl)quinolin-7-yl]ethanone (0.0287 g, 0.0936 mmol) and ammonium acetate (0.0721 g, 0.936 mmol) in methanol (1.0 mL) and acetonitrile (1.0 mL) was heated at 65° C. in a sealed tube for 1 hour. After cooling to room temperature, to the resulting mixture was added 1.0 M sodium cyanoborohydride in tetrahydrofuran (0.234 mL, 0.234 mmol). The reaction was heated at 65° C. overnight. The mixture was cooled to room temperature, quenched with sat. NaHCO3 solution and extracted with dichloromethane. The combined organic layers were dried over MgSO4 and concentrated to give the desired product. LCMS calculated for C16H20ClFN3 (M+H)+: m/z=308.1; Found: 308.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08680108B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-67f862a6cabd4ba0badaa442e147f97e |
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| Source note | uspto-grants-2014_03 |
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