4-(1-Piperazinyl)benzamide → HCID 19911464, compound

HRID 1533934Notes

Reaction equation

HRID 1533934 reaction equation
Cl[CH2:2][CH2:3][CH:4]1[O:8][C:7](=[O:9])[N:6]([CH3:10])[CH2:5]1.[N:11]1([C:17]2[CH:25]=[CH:24][C:20]([C:21]([NH2:23])=[O:22])=[CH:19][CH:18]=2)[CH2:16][CH2:15][NH:14][CH2:13][CH2:12]1>>[CH3:10][N:6]1[CH2:5][CH:4]([CH2:3][CH2:2][N:14]2[CH2:13][CH2:12][N:11]([C:17]3[CH:18]=[CH:19][C:20]([C:21]([NH2:23])=[O:22])=[CH:24][CH:25]=3)[CH2:16][CH2:15]2)[O:8][C:7]1=[O:9]

Participants

3

Reactant 2

HCID 111065094-(1-Piperazinyl)benzamideHCID 146987465-(2-Chloro-ethyl)-3-methyl-oxazolidin-2-one

Product 1

HCID 19911464HCID 19911464, compound

Procedure

Following the procedure of Example 2, the title compound is prepared from 5-(2-chloroethyl)-3-methyl-2-oxazolidinone and 4-(1-piperazinyl)benzamide.

Sources & evidence

ORD record
ord-e28c1f372a5c4eb8b46d4f8b3d2db94c
Source dataset
uspto-grants-1992_02
Patent number
US05086055

Reaction notes

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