HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893276Generated: October 29, 2026
Dimethylformamide → HCID 19891963, compound
https://huagongshe.com/reaction/893276
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (1-Methyl-2-piperidinyl)methyl 1H-indole-3-carboxylate | HCID 19891949 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19891963 | HCID 19891963 | — |
Reaction Steps
To a DMF (10 ml) suspension of 60% sodium hydride (0.09 g, 2.3 mmol) was dropwise added a DMF (5 ml) solution of (1-methyl-2-piperidyl)methyl 1H-indole-3-carboxylate (0.50 g, 1.8 mmol) at room temperature over a period of 5 min. Onto the reaction mixture stirred for 15 min. was poured a THF (5 ml) solution of methyl iodide (0.29 g, 2.0 mmol). After stirring overnight, a reaction solution was poured onto water followed by extraction with EtOAc. The organic layer was washed successively with water and saturated aqueous sodium chloride, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude product thus produced was purified by column chromatography on silica gel (20 g, CHCl3) to give 0.43 g of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05124324 |
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| Source dataset | uspto-grants-1992_06 |
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| ORD ID | ord-6595af5a7b85409e96adf005835ca59f |
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| Source note | uspto-grants-1992_06 |
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