1-[2-(Pyrrolidin-1-yl)ethyl]piperazine → 4-(2-Benzoyl-phenylsulfamoyl)-N-{2-oxo-2-[4-(2-pyrrolidin-1-yl-ethyl)-piperazin-1-yl]-ethyl}-benzamide

HRID 446865Notes

Reaction equation

HRID 446865 reaction equation
[C:1]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[NH:15][S:16]([C:19]1[CH:31]=[CH:30][C:22]([C:23]([NH:25][CH2:26][C:27]([OH:29])=O)=[O:24])=[CH:21][CH:20]=1)(=[O:18])=[O:17])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[N:32]1([CH2:37][CH2:38][N:39]2[CH2:44][CH2:43][NH:42][CH2:41][CH2:40]2)[CH2:36][CH2:35][CH2:34][CH2:33]1>>[C:1]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[NH:15][S:16]([C:19]1[CH:31]=[CH:30][C:22]([C:23]([NH:25][CH2:26][C:27](=[O:29])[N:42]2[CH2:41][CH2:40][N:39]([CH2:38][CH2:37][N:32]3[CH2:33][CH2:34][CH2:35][CH2:36]3)[CH2:44][CH2:43]2)=[O:24])=[CH:21][CH:20]=1)(=[O:17])=[O:18])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

3

Procedure

The title compound was prepared from [4-(2-benzoyl-phenylsulfamoyl)-benzoylamino]-acetic acid and 1-(2-pyrrolidin-1-yl-ethyl)-piperazine (EMKA-Chemie) according to the method described in Example 1.1/f. MS (EI) 604.2 (MH+).

Sources & evidence

ORD record
ord-d8a796f53c144e4d9480d2b2b930d292
Source dataset
uspto-grants-2013_07
Patent number
US08481527B2

Reaction notes

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