HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804753Generated: November 1, 2026
Water → 5-Bromo-1-methyl-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine
https://huagongshe.com/reaction/1804753
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Bromo-2,3-dihydro-7-azaindole | HCID 21964079 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Bromo-1-methyl-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine | HCID 58730933 | — |
Reaction Steps
To a suspension stirred at 0° C., under an inert atmosphere, of 0.48 g (12.06 mmol) of 60% sodium hydride in 5 mL of dimethylformamide is added dropwise a solution of 5-bromo-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine in 10 mL of dimethylformamide. The mixture is stirred at 0° C. for 15 minutes and then at 20° C. for 45 minutes. A solution of 0.77 mL (12.06 mmol) of methyl iodide in 5 mL of dimethylformamide is then added to this stirred suspension at 0° C. The mixture is then stirred for 48 hours. After this time, 50 mL of water and 50 mL of ethyl acetate are added to the mixture. The aqueous phase is separated out and then extracted with 3×30 mL of ethyl acetate. The organic phases are combined, washed with 2×50 mL of water and then concentrated under reduced pressure. The resulting product is purified by chromatography on a column of silica, eluting with a mixture of dichloromethane and methanol. 0.97 g of the expected product is thus isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354425B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-5173dcd9f77049799a8d9b1b2ac6a774 |
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| Source note | uspto-grants-2013_01 |
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