HCID 18789311, compound → HCID 18789287, compound
Reaction equation
Br[C:2]1[CH:7]=[CH:6][C:5]([C:8]2[NH:12][N:11]=[C:10]([NH:13][C:14]([CH:16]3[CH2:24][C:23]4[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=4)[CH2:17]3)=[O:15])[CH:9]=2)=[CH:4][CH:3]=1.Br[C:26]1C=C(C2NN=C(NC(C3CC4C(=CC=CC=4)C3)=O)C=2)C=C[CH:31]=1>>[CH2:17]1[C:18]2[C:23](=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH2:24][CH:16]1[C:14]([NH:13][C:10]1[CH:9]=[C:8]([C:5]2[CH:6]=[CH:7][CH:2]=[C:3]([CH:26]=[CH2:31])[CH:4]=2)[NH:12][N:11]=1)=[O:15]Participants
3
Procedure
The title compound was prepared in the same manner as that described in Example 33 except that 5-(4-bromophenyl)-3-(2-indanyl)carbonylaminopyrazole used in Example 33 was replaced with 5-(3-bromophenyl)-3-(2-indanyl)carbonylaminopyrazole.
Sources & evidence
- ORD record
- ord-53656140f454404da393bab5515aa6f7
- Source dataset
- uspto-grants-2000_05
- Patent number
- US06057335
Reaction notes
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