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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylazodicarboxamideHCID 4278—
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriphenylphosphineHCID 11776—
Reactanttert-butyl N-(2-hydroxyethyl)carbamateHCID 2733206—
Reactant6-Methoxy-1-(phenylsulfonyl)-1H-indol-5-olHCID 67241682—
SolventDichloromethaneHCID 6344—
Product2-{[6-Methoxy-1-(phenylsulfonyl)-1H-indol-5-yl]oxy}ethanamineHCID 67241887110.7%

Reaction Conditions

Temperature150 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960374B2
Source datasetuspto-grants-2011_06
ORD IDord-158f3b77cef44415a896850bbc800ec2
Source noteuspto-grants-2011_06