HCID 874532, compound → HCID 57762810, compound
Reaction equation
I[C:2]1[CH:7]=[CH:6][C:5]([S:8]([N:11]2[CH2:15][CH2:14][CH2:13][CH2:12]2)(=[O:10])=[O:9])=[CH:4][CH:3]=1.[F:16][C:17]([F:28])([F:27])[C:18]1[C:26]2[CH2:25][CH2:24][CH2:23][CH2:22][C:21]=2[NH:20][N:19]=1>>[N:11]1([S:8]([C:5]2[CH:6]=[CH:7][C:2]([N:20]3[C:21]4[CH2:22][CH2:23][CH2:24][CH2:25][C:26]=4[C:18]([C:17]([F:16])([F:28])[F:27])=[N:19]3)=[CH:3][CH:4]=2)(=[O:10])=[O:9])[CH2:15][CH2:14][CH2:13][CH2:12]1Participants
3
Procedure
The title compound was prepared from 1-[(4-iodophenyl)sulfonyl]pyrrolidine and 3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazole using a similar procedure to that described for Example 87.
Sources & evidence
- ORD record
- ord-889c511e9bd3489bbd006a13d1de9576
- Source dataset
- uspto-grants-2010_01
- Patent number
- US07642256B2
Reaction notes
Loading…