HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400726Generated: October 27, 2026
Methyl iodide → 1-methyl-1H-indole-5-carbonitrile
https://huagongshe.com/reaction/400726
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | 5-Bromoindole | HCID 24905 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-methyl-1H-indole-5-carbonitrile | HCID 11412513 | 70% |
Reaction Steps
A mixture of 5-bromoindole (500 mg; 2.55 mmol) and cuprous cyanide (342 mg; 3.83 mmol) in NMP (10 mL) was heated under microwave irradiations to 100° C. for 30 minutes then at 200° C. for 30 minutes. The reaction mixture was partitioned with water and DCM and the organic layer was washed with brine and concentrated in vacuo to give a pink solid. Purification by silica column chromatography (DCM) gave a white solid. It was dissolved in DMF (5 mL) and K2CO3 (704 mg; 5.10 mmol) and iodomethane (543 mg; 3.83 mmol) were successively added. The reaction mixture was stirred at RT for 3 days and then partitioned between water and EtOAc. The organic layer was washed with brine, dried over MgSO4 and concentrated under vacuum to give a slightly yellow oil which crystallized upon standing to give the title compound as an off-white solid (80 mg, 70%). LC/MS (Method A): 156.9 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741923B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-2d1a23f06efe4132a2780d890867b159 |
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| Source note | uspto-grants-2014_06 |
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