Piperidin-1-yl-acetic acid → HCID 21105560, compound
Reaction equation
[CH:1]1([O:6][C:7]2[CH:12]=[CH:11][C:10]([NH:13][C:14]([NH:16][C:17]3[CH:22]=[CH:21][C:20]([N:23]4[CH2:27][CH2:26][CH:25]([NH:28][CH3:29])[CH2:24]4)=[CH:19][CH:18]=3)=[O:15])=[CH:9][CH:8]=2)[CH2:5][CH2:4][CH2:3][CH2:2]1.[N:30]1([CH2:36][C:37]([OH:39])=O)[CH2:35][CH2:34][CH2:33][CH2:32][CH2:31]1>>[CH:1]1([O:6][C:7]2[CH:8]=[CH:9][C:10]([NH:13][C:14](=[O:15])[NH:16][C:17]3[CH:22]=[CH:21][C:20]([N:23]4[CH2:27][CH2:26][CH:25]([N:28]([CH3:29])[C:37](=[O:39])[CH2:36][N:30]5[CH2:31][CH2:32][CH2:33][CH2:34][CH2:35]5)[CH2:24]4)=[CH:19][CH:18]=3)=[CH:11][CH:12]=2)[CH2:2][CH2:3][CH2:4][CH2:5]1Participants
3
Procedure
1-(4-Cyclopentyloxyphenyl)-3-[4-(3-methylaminopyrrolidin-1-yl)phenyl]urea was reacted with piperidin-1-ylacetic acid by method E. This resulted in the product with the molecular weight of 519.69 (C30H41N5O3); MS (ESI): 520 (M+H+).
Workup
- customThis resulted in the product with the molecular weight of 519.69 (C30H41N5O3)
Sources & evidence
- ORD record
- ord-f16070215757446c8de17cf996e29137
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07968550B2
Reaction notes
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