HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719375Generated: October 26, 2026
Water → 1-(5-Methoxycarbonylpentyl)-2-(1-imidazolyl)-3-methylindole
https://huagongshe.com/reaction/1719375
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 6-Bromohexanoate | HCID 4170292 | — |
| Reactant | 2-(1-Imidazolyl)-3-methylindole | HCID 13280839 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(5-Methoxycarbonylpentyl)-2-(1-imidazolyl)-3-methylindole | HCID 13280840 | — |
Reaction Steps
To a suspension of 60% sodium hydride (0.34 g) in dimethylformamide (10 ml), while stirring under nitrogen at 0°-5°, is added dropwise a solution of 2-(1-imidazolyl)-3-methyl-indole (1.50 g) in dimethylformamide (15 ml). Upon complete addition the mixture is stirred at 0°-5° for 1 hour. To the nearly complete solution is added methyl 6-bromohexanoate (1.67 g) dropwise. The mixture is stirred at 0°-5° for 0.5 hour, then for two days at room temperature. The solution is poured into water (100 ml) and extracted with ethyl acetate (3×50 ml), dried (MgSO4), filtered, and concentrated in vacuo to give an amber oil which is stirred with 100 ml of petroleum ether for 15 minutes. The mixture is placed in a separatory funnel and the insoluble amber oil separated and removed. The oil is dried in vacuo to give 1-(5-methoxycarbonylpentyl)-2-(1-imidazolyl)-3-methylindole as an oil; NMR (CDCl3): δ3.60 (3H), 3.90 (2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04539410 |
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| Source dataset | uspto-grants-1985_09 |
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| ORD ID | ord-883c870e4fa14a388b28fe1f6e7cd786 |
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| Source note | uspto-grants-1985_09 |
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