HCID 178418806, compound → HCID 178517071, compound
Reaction equation
NC1C=CNN=1.O/[CH:8]=[C:9]1\[C:10](=[O:18])[NH:11][C:12]2[C:17]\1=[CH:16][CH:15]=[CH:14][CH:13]=2.Cl.[CH2:20]([O:27][C:28]1[CH:29]=[C:30]([C:42]2[CH:43]=[C:44]([NH2:47])[NH:45][N:46]=2)[CH:31]=[C:32]([O:34][CH2:35][C:36]2[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=2)[CH:33]=1)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>O1CCCC1>[CH2:35]([O:34][C:32]1[CH:31]=[C:30]([C:42]2[CH:43]=[C:44]([NH:47][CH:8]=[C:9]3[C:17]4[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=4)[NH:11][C:10]3=[O:18])[NH:45][N:46]=2)[CH:29]=[C:28]([O:27][CH2:20][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[CH:33]=1)[C:36]1[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The named compound is prepared by substituting 5-(3,5-bis-benzyloxy-phenyl)-2H-pyrazol-3-ylamine hydrochloride for 3-aminopyrazole in the reaction of Example 1. Specifically, E & Z-3-[(hydroxy)-methylene]-1,3-dihydro-indol-2-one (0.030 gms.) is reacted with 0.114 gms. of 5-(3,5-bis-benzyloxy-phenyl)-2H-pyrazol-3-ylamine hydrochloride by refluxing in tetrahydrofuran (2.0 mL).
Workup
- customThe named compound is prepared
- customin the reaction of Example 1
Sources & evidence
- ORD record
- ord-261e4a1b289245eab070394febbbc9e1
- Source dataset
- uspto-grants-2006_02
- Patent number
- US07005444B2
Reaction notes
Loading…