3-Cyclopentylpropionyl chloride → 5-[(3-Cyclopentylpropanoyl)(4-{[(4-pentylbenzyl)amino]carbonyl}benzyl)amino]-2-hydroxybenzoic acid
Reaction equation
[CH2:1]([C:6]1[CH:13]=[CH:12][C:9]([CH2:10][NH2:11])=[CH:8][CH:7]=1)[CH2:2][CH2:3][CH2:4][CH3:5].Cl[CH2:15][C:16]1[CH:24]=[CH:23][C:19]([C:20](Cl)=[O:21])=[CH:18][CH:17]=1.[CH:25]1([CH2:30][CH2:31][C:32](Cl)=[O:33])[CH2:29][CH2:28][CH2:27][CH2:26]1.[NH2:35][C:36]1[CH:48]=[CH:47][C:39]2[O:40]C(C)(C)[O:42][C:43](=[O:44])[C:38]=2[CH:37]=1>>[CH:25]1([CH2:30][CH2:31][C:32]([N:35]([CH2:15][C:16]2[CH:24]=[CH:23][C:19]([C:20]([NH:11][CH2:10][C:9]3[CH:12]=[CH:13][C:6]([CH2:1][CH2:2][CH2:3][CH2:4][CH3:5])=[CH:7][CH:8]=3)=[O:21])=[CH:18][CH:17]=2)[C:36]2[CH:48]=[CH:47][C:39]([OH:40])=[C:38]([CH:37]=2)[C:43]([OH:44])=[O:42])=[O:33])[CH2:29][CH2:28][CH2:27][CH2:26]1Participants
5
Reactant 4
Product 1
Procedure
The title compound was prepared following the procedure A using 4-pentylbenzylamine, 4-(chloromethyl)benzoyl chloride, 3-cyclopentylpropanoyl chloride and 6-amino-2,2-dimethyl-4H-1,3-benzodioxin-4-one. M+(ESI): 571.6
Sources & evidence
- ORD record
- ord-c030b86011354738bd28e13aa3a863ca
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07365225B2
Reaction notes
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