2-Amino-5-bromo-1,3,4-thiadiazole → N-[3-[3-[(4-Methyl-1-piperazinyl)methyl]phenoxy]propyl]1,3,4-thiadiazole-2,5-diamine
Reaction equation
[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([CH2:8][C:9]2[CH:10]=[C:11]([CH:17]=[CH:18][CH:19]=2)[O:12][CH2:13][CH2:14][CH2:15][NH2:16])[CH2:4][CH2:3]1.Br[C:21]1[S:25][C:24]([NH2:26])=[N:23][N:22]=1>>[CH3:1][N:2]1[CH2:3][CH2:4][N:5]([CH2:8][C:9]2[CH:10]=[C:11]([CH:17]=[CH:18][CH:19]=2)[O:12][CH2:13][CH2:14][CH2:15][NH:16][C:21]2[S:25][C:24]([NH2:26])=[N:23][N:22]=2)[CH2:6][CH2:7]1Participants
3
Procedure
The compound is prepared by a method analogous to that of Example 51 from 3-[3-[(4-methyl-1-piperazinyl) methyl]phenoxy]-1-propanamine and 5-bromo-1,3,4-thiadiazole-2-amine.
Sources & evidence
- ORD record
- ord-c23299e4c56f495ea8bb7cfb36122b35
- Source dataset
- uspto-grants-1988_02
- Patent number
- US04727081
Reaction notes
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