Benzenemethanol, alpha-cyclopropyl-alpha-methyl-4-(trifluoromethyl)- → 3-{1-Cyclopropyl-1-[4-(trifluoromethyl)phenyl]ethyl}-7-[(methylsulfanyl)methyl]-1H-indole
Reaction equation
[CH3:1][S:2][CH2:3][C:4]1[CH:5]=[CH:6][CH:7]=[C:8]2[C:12]=1[NH:11][CH:10]=[CH:9]2.[CH:13]1([C:16]([C:19]2[CH:24]=[CH:23][C:22]([C:25]([F:28])([F:27])[F:26])=[CH:21][CH:20]=2)(O)[CH3:17])[CH2:15][CH2:14]1.ClC1C=CC(C(C2C3C(=C(CSC)C=CC=3)NC=2)(C2CC2)C)=CC=1>>[CH:13]1([C:16]([C:9]2[C:8]3[C:12](=[C:4]([CH2:3][S:2][CH3:1])[CH:5]=[CH:6][CH:7]=3)[NH:11][CH:10]=2)([C:19]2[CH:20]=[CH:21][C:22]([C:25]([F:26])([F:27])[F:28])=[CH:23][CH:24]=2)[CH3:17])[CH2:15][CH2:14]1Participants
4
Reactant 3
Product 1
Procedure
The title compound was prepared starting from 462 mg (2.61 mmol) of the compound from Example 8A and 600 mg (2.61 mmol) of the compound from Example 139A in analogy to the synthesis of the compound from Example 184. 273 mg (27% of theory) of the target compound were obtained.
Workup
- custom273 mg (27% of theory) of the target compound were obtained
Sources & evidence
- ORD record
- ord-7fc8426b095e48da80055c39e77035f8
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08063234B2
Reaction notes
Loading…