HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37944Generated: October 30, 2026
HCID 66640061, compound → HCID 66640764, compound
https://huagongshe.com/reaction/37944
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 66640061 | HCID 66640061 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Trifluoroacetic acid methylene chloride | HCID 21863450 | — |
| Product | HCID 66640764 | HCID 66640764 | 88.2% |
Reaction Steps
A solution of 6-(benzyl-methyl-amino)-3-(cyano-dimethyl-methyl)-indole-1-carboxylic acid tert-butyl ester (26.4 g, 90%, 58.9 mmol) in DCM-TFA (2:1, 180 mL) was stirred for 20 h at 20° C. Evaporation of solvent gave a crude, which was redissolved in DCM and the solution was washed with water, aqueous sodium bicarbonate and water and dried over MgSO4. Evaporation of solvent gave a solid, which was triturated with hexane to give [6-(benzyl-methyl-amino)-1H-indol-3-yl]-acetonitrile as a solid (14.3 g). MS (ES): 304 (MH+). [6-(benzyl-methyl-amino)-1H-indol-3-yl]-acetonitrile was then treated in a manner similar to that described in Step 34D-H, but using greater than three equivalents of iodomethane, to give 6-(benzyl(methyl)amino)-1,1-dimethyl-1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylic acid ethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524704B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-3376733973064c89bd19bb001decd1a7 |
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| Source note | uspto-grants-2013_09 |
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