HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192562Generated: November 2, 2026
Ammonium Acetate → 1-[8-(3-Fluorophenyl)-5-methylquinolin-7-yl]ethanamine
https://huagongshe.com/reaction/1192562
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 1-[8-(3-Fluorophenyl)-5-methylquinolin-7-yl]ethanone | HCID 58368662 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-[8-(3-Fluorophenyl)-5-methylquinolin-7-yl]ethanamine | HCID 58368628 | — |
Reaction Steps
A mixture of 1-[8-(3-fluorophenyl)-5-methylquinolin-7-yl]ethanone (50 mg, 0.2 mmol) and ammonium acetate (138 mg, 1.79 mmol) in methanol (1.0 mL) and acetonitrile (1.0 mL) was heated at 65° C. in a sealed tube for 30 minutes. After cooling to room temperature, sodium cyanoborohydride (22.5 mg, 0.358 mmol). The reaction was heated at 65° C. for another 4 hours, then cooled to room temperature and quenched with sat. sodium bicarbonate, extracted with dichloromethane. The combined extracts were dried over magnesium sulfate and evaporated to dryness. The residue was used directly in the next step. LCMS calculated for C18H18FN2 (M+H)+: m/z=281.1; Found: 281.1.
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-df7050142b4740a19076534e87656050 |
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| Source note | uspto-grants-2014_03 |
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