2-(2-Dimethylaminoethylthio)-4-nitroanisole → 4-Amino-2-(2-dimethylaminoethylthio)anisole
Reaction equation
[CH3:1][N:2]([CH3:17])[CH2:3][CH2:4][S:5][C:6]1[CH:11]=[C:10]([N+:12]([O-])=O)[CH:9]=[CH:8][C:7]=1[O:15][CH3:16].CC1C=C(C2C=NC=CN=2)C=CC=1C1C=CC(C(O)=O)=CC=1>>[NH2:12][C:10]1[CH:9]=[CH:8][C:7]([O:15][CH3:16])=[C:6]([S:5][CH2:4][CH2:3][N:2]([CH3:1])[CH3:17])[CH:11]=1Participants
3
Procedure
The title compound was prepared from 2-(2-dimethylaminoethylthio)-4-nitroanisole (D47) (788 mg) using a similar procedure to Description 2 (88%).
Sources & evidence
- ORD record
- ord-17b8010158e04aeea01c8f4833191143
- Source dataset
- uspto-grants-1998_09
- Patent number
- US05801170
Reaction notes
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