HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423183Generated: October 31, 2026
N,N,N',N'-Tetramethylazodicarboxamide → 2-{[6-Methoxy-1-(phenylsulfonyl)-1H-indol-5-yl]oxy}ethanamine
https://huagongshe.com/reaction/2423183
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N,N',N'-Tetramethylazodicarboxamide | HCID 4278 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | tert-butyl N-(2-hydroxyethyl)carbamate | HCID 2733206 | — |
| Reactant | 6-Methoxy-1-(phenylsulfonyl)-1H-indol-5-ol | HCID 67241682 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-{[6-Methoxy-1-(phenylsulfonyl)-1H-indol-5-yl]oxy}ethanamine | HCID 67241887 | 110.7% |
Reaction Steps
To 6-methoxy-1-(phenylsulfonyl)-1H-indol-5-ol (Intermediate 15, 2.0 g, 6.6 mmol), 1,1′-azobis(N,N-dimethylformamide) (2.3 g, 13 mmol), triphenylphosphine (3.5 g, 13 mmol), tert-butyl N-(2-hydroxy-ethyl)carbamate (2.1 g, 13 mmol) and DCM (40 mL) were added. The mixture was heated at 150° C. for 20 minutes in a microwave heater. The reaction mixture was allowed to cool to room temperature and TFA (30 mL) was added. The reaction mixture was allowed to stir at room temperature for 30 minutes. The solvent was removed under reduced pressure and the crude material was purified by flash chromatography on silica gel using 5% MeOH in DCM as the eluent to afford the title compound (2.53 g) MS m/z 347 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07960374B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-158f3b77cef44415a896850bbc800ec2 |
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| Source note | uspto-grants-2011_06 |
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