4-(4-Methylpiperazin-1-yl)aniline → 1-(4-Isothiocyanatophenyl)-4-methylpiperazine
Reaction equation
[N:1]([C:4]1[CH:17]=[CH:16][C:7](OCCN2CCCC2)=[CH:6][CH:5]=1)=[C:2]=[S:3].[CH3:18][N:19]1[CH2:24][CH2:23][N:22](C2C=CC(N)=CC=2)[CH2:21][CH2:20]1>>[N:1]([C:4]1[CH:5]=[CH:6][C:7]([N:22]2[CH2:23][CH2:24][N:19]([CH3:18])[CH2:20][CH2:21]2)=[CH:16][CH:17]=1)=[C:2]=[S:3]Participants
3
Procedure
The title compound is prepared as described in Example 1 for 1-[2-(4-isothiocyanato-phenoxy)-ethyl]-pyrrolidine but using 4-(4-methyl-piperazin-1-yl)-phenylamine. Title compound: ES-MS: 234.0 [M+H]+; single peak at tR=6.60 min (System 1).
Workup
- customThe title compound is prepared
Sources & evidence
- ORD record
- ord-8964d51a763949d59a6ebb703185b2e4
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07795288B2
Reaction notes
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