4-(3-Chloro-2-hydroxypropyl)-1-diphenylmethylpiperazine → 5-[3-(4-Diphenylmethylpiperazine-1-yl)-2-hydroxypropylthio]quinoline
Reaction equation
[N:1]1[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([SH:11])[C:5]=2[CH:4]=[CH:3][CH:2]=1.Cl[CH2:13][CH:14]([OH:35])[CH2:15][N:16]1[CH2:21][CH2:20][N:19]([CH:22]([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[CH2:18][CH2:17]1>>[C:29]1([CH:22]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[N:19]2[CH2:18][CH2:17][N:16]([CH2:15][CH:14]([OH:35])[CH2:13][S:11][C:6]3[CH:7]=[CH:8][CH:9]=[C:10]4[C:5]=3[CH:4]=[CH:3][CH:2]=[N:1]4)[CH2:21][CH2:20]2)[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=1Participants
3
Procedure
Following the same procedure as in Example 23-(c), reaction and treatment were carried out using 220 mg of 5-quinolinethiol and 1.2 g of 4-(3-chloro-2-hydroxypropyl)-1-(diphenylmethyl)piperazine, in order to obtain 130 mg of 5-[3-(4-diphenylmethylpiperazine-1-yl)-2-hydroxyProPylthio]quinoline.
Workup
- customas in Example 23-(c), reaction and treatment
Sources & evidence
- ORD record
- ord-8cf9ff785e5b409da86cdf46b0191eb4
- Source dataset
- uspto-grants-1995_04
- Patent number
- US05405843
Reaction notes
Loading…