HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83643Generated: October 28, 2026
Isobutyl iodide → HCID 66571466, compound
https://huagongshe.com/reaction/83643
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isobutyl iodide | HCID 10556 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-benzyl-1-(1H-indole-2-carbonyl)-N-methylpiperidine-4-carboxamide | HCID 66571403 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66571466 | HCID 66571466 | — |
Reaction Steps
N-benzyl-1-(1H-indole-2-carbonyl)-N-methylpiperidine-4-carboxamide (100 mg, 0.266 mmol) was dissolved in 1.0 mL of DMF and added to a suspension of sodium hydride (12.78 mg, 0.320 mmol) in 2.0 mL of DMF. The reaction was stirred at 80° C. for 10 minutes before adding 1-iodo-2-methylpropane (0.061 mL, 0.533 mmol). The reaction was allowed to stir overnight. After 18 hours, the reaction was cooled to room temperature before diluting with water and ethyl acetate. The organic phase was washed with water followed by saturated sodium chloride, dried over magnesium sulfate, filtered and concentrated. The crude material was purified via column chromatography using 50% ethyl acetate/hexanes to 100% ethyl acetate. The purification provided product as a white solid. (Yield: 28 mg, white solid) 1H-NMR (400 MHz, DMSO-d6) 7.64-7.51, 7.43-7.16, 7.11-7.03, 6.71-6.61, 4.67, 4.51, 4.19-4.07, 3.13-2.91, 2.79, 2.06-1.93, 1.88-1.50, 0.84-0.73
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846684B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-66bfe81d4dcb410daaba05483a497893 |
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| Source note | uspto-grants-2014_09 |
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