Reaction equation
Cl[S:2]([C:5]1[CH:14]=[CH:13][C:8]([C:9]([O:11][CH3:12])=[O:10])=[CH:7][CH:6]=1)(=[O:4])=[O:3].[CH2:15]([N:17]1[C:25]2[C:20](=[CH:21][C:22]([CH2:26][NH2:27])=[CH:23][CH:24]=2)[CH:19]=[N:18]1)[CH3:16]>>[CH2:15]([N:17]1[C:25]2[C:20](=[CH:21][C:22]([CH2:26][NH:27][S:2]([C:5]3[CH:14]=[CH:13][C:8]([C:9]([O:11][CH3:12])=[O:10])=[CH:7][CH:6]=3)(=[O:4])=[O:3])=[CH:23][CH:24]=2)[CH:19]=[N:18]1)[CH3:16]Participants
3
Procedure
The titled compound was prepared according to the procedure described in step-1 of Example 1 from methyl 4-(chlorosulfonyl)benzoate and (1-ethyl-1H-indazol-5-yl)methanamine (step-3 of Example 14).
Sources & evidence
- ORD record
- ord-13e5a233b3cf492a8a0862b53f86176a
- Source dataset
- uspto-grants-2014_09
- Patent number
- US08829026B2
Linked notes
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