4-Hydroxy-4-thiazol-2-yl-cyclohexanone → HCID 54755922, compound
Reaction equation
OC(C(F)(F)F)=O.[C:8]([NH:12][C:13]([N:15]1[C:23]2[C:18](=[CH:19][C:20]([C:24]([F:27])([F:26])[F:25])=[CH:21][CH:22]=2)[C:17]([NH:28][CH2:29][C:30](=[O:36])[NH:31][CH:32]2[CH2:35][NH:34][CH2:33]2)=[N:16]1)=[O:14])([CH3:11])([CH3:10])[CH3:9].[OH:37][C:38]1([C:45]2[S:46][CH:47]=[CH:48][N:49]=2)[CH2:43][CH2:42][C:41](=O)[CH2:40][CH2:39]1>>[C:8]([NH:12][C:13]([N:15]1[C:23]2[C:18](=[CH:19][C:20]([C:24]([F:26])([F:25])[F:27])=[CH:21][CH:22]=2)[C:17]([NH:28][CH2:29][C:30](=[O:36])[NH:31][CH:32]2[CH2:33][N:34]([CH:41]3[CH2:40][CH2:39][C:38]([OH:37])([C:45]4[S:46][CH:47]=[CH:48][N:49]=4)[CH2:43][CH2:42]3)[CH2:35]2)=[N:16]1)=[O:14])([CH3:11])([CH3:9])[CH3:10]Participants
3
Procedure
The title compound was prepared as a white solid from reaction of 3-[(azetidin-3-ylcarbamoylmethyl)-amino]-5-trifluoromethyl-indazole-1-carboxylic acid tert-butyl amide TFA salt and 4-hydroxy-4-thiazol-2-yl-cyclohexanone using the procedure described in Step E of Example 1.
Sources & evidence
- ORD record
- ord-11bd5ddb905c408aa1f8a378eddfe224
- Source dataset
- uspto-grants-2013_05
- Patent number
- US08436023B2
Reaction notes
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