4-(3-Chloro-2-hydroxypropyl)-1-diphenylmethylpiperazine → HCID 20079035, compound

HRID 1590650Notes

Reaction equation

HRID 1590650 reaction equation
[Cl:1][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][C:8]=2[OH:12])[N:3]=1.Cl[CH2:14][CH:15]([OH:36])[CH2:16][N:17]1[CH2:22][CH2:21][N:20]([CH:23]([C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)[C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[CH2:19][CH2:18]1>>[Cl:1][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][C:8]=2[O:12][CH2:14][CH:15]([OH:36])[CH2:16][N:17]2[CH2:18][CH2:19][N:20]([CH:23]([C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=3)[C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)[CH2:21][CH2:22]2)[N:3]=1

Participants

3

Reactant 2

HCID 103601754-(3-Chloro-2-hydroxypropyl)-1-diphenylmethylpiperazineHCID 1354422212-chloroquinolin-5-ol

Product 1

HCID 20079035HCID 20079035, compoundYield 51.2%

Procedure

Following the same procedure as in Example 23-(c), reaction and treatment were carried out using 1 g of 2-chloro-5-hydroxyquinoline and 2.88 g of 4-(3-chloro-2-hydroxypropyl)-1-diphenylmethylpiperazine synthesized in Example 23-(b), in order to obtain 1.39 g of 2-chloro-5-[3-(4-diphenylmethylpiperazine-1-yl)-2-hydroxypropoxy]quinoline.

Workup

  1. customas in Example 23-(c), reaction and treatment

Sources & evidence

ORD record
ord-674f640752bf4bf1991077250c632892
Source dataset
uspto-grants-1993_04
Patent number
US05204348

Reaction notes

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