HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818618Generated: November 3, 2026
Methyl iodide → 1-(5-chloro-1-methyl-1H-indol-2-yl)heptan-1-one
https://huagongshe.com/reaction/1818618
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 66777278 | HCID 66777278 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(5-chloro-1-methyl-1H-indol-2-yl)heptan-1-one | HCID 66777768 | — |
Reaction Steps
To a solution of the title compound of Example 1 Step B (98.0 mg, 0.37 mmol) in DMF was added NaH (15.0 mg, 60% suspension in mineral oil, 0.37 mmol). After 10 min, iodomethane (0.023 mL, 0.37 mmol) was added, and the mixture was stirred for 2 h, whereupon it was quenched by addition of sat. aq. NaHCO3. The aqueous phase was extracted with EtOAc, and the organic phase was concentrated in vacuo. Purification by flash chromatography on silica gel (0 to 10%, then 10 to 100% EtOAc in hexanes) provided the title compound: LCMS C, tr=2.78 min, m/z 278.3 [M+H]+; 1H NMR (500 MHz, CDCl3) δ 7.65 (app t, J=1.0 Hz, 1H), 7.31 (d, J=1.0 Hz, 2H), 7.20 (s, 1H), 4.05 (s, 3H), 2.95 (t, J=7.0 Hz, 2H), 1.79-1.72 (m, 2H), 1.43-1.26 (m, 6H), 0.90 (t, J=7.5 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07598398B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-516fbe1fbccd48d7b020e381d331f554 |
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| Source note | uspto-grants-2009_10 |
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