HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175346Generated: October 29, 2026
Ammonium Acetate → 1-[1-(3-Fluorophenyl)-3-methyl-1H-indol-2-yl]ethanamine
https://huagongshe.com/reaction/2175346
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 1-[1-(3-Fluorophenyl)-3-methyl-1H-indol-2-yl]ethanone | HCID 58565366 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-[1-(3-Fluorophenyl)-3-methyl-1H-indol-2-yl]ethanamine | HCID 58565351 | 96.6% |
Reaction Steps
A mixture of 1-[1-(3-fluorophenyl)-3-methyl-1H-indol-2-yl]ethanone (0.165 g, 0.617 mmol) and ammonium acetate (0.476 g, 6.17 mmol) in methanol (2.0 mL) and acetonitrile (2.0 mL) was heated at 65° C. in a sealed tube for 1 hour. After cooling to room temperature, sodium cyanoborohydride (0.12 g, 1.9 mmol) was added to the resultant mixture. The reaction was heated at 65° C. over the weekend. The reaction was cooled to room temperature and quenched with saturated NaHCO3 solution and then extracted with dichloromethane, dried over MgSO4 and concentrated to give the crude amine (0.16 g), which was used directly in next step. LCMS calculated for C17H18FN2(M+H)+: m/z=269.1. Found: 252.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09062055B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-d0f917a4a43740829fa8f313a35afcb8 |
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| Source note | uspto-grants-2015_06 |
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