Triethylsilane → HCID 19974138, compound
Reaction equation
O[CH2:2][CH2:3][NH:4][CH2:5][CH2:6][C:7]1[CH:12]=[CH:11][C:10]([O:13][CH3:14])=[CH:9][CH:8]=1.[F:15][C:16]([F:27])([F:26])[C:17]1[S:18][CH:19]=[C:20]([C:22](=[O:25])[CH2:23]Br)[N:21]=1.C([SiH](CC)CC)C>>[CH3:14][O:13][C:10]1[CH:11]=[CH:12][C:7]([CH2:6][CH2:5][N:4]2[CH2:3][CH2:2][O:25][CH:22]([C:20]3[N:21]=[C:17]([C:16]([F:27])([F:26])[F:15])[S:18][CH:19]=3)[CH2:23]2)=[CH:8][CH:9]=1Participants
4
Procedure
Prepared analogously to Example 32 by reaction of N-(2-hydroxyethyl)-2-(4-methoxyphenyl)ethanamine with 2-trifluoromethyl-4-bromoacetyl-thiazole followed by reduction with triethylsilane.
Sources & evidence
- ORD record
- ord-0a4e095c29614321986dd0b49ab762de
- Source dataset
- uspto-grants-1989_12
- Patent number
- US04886814
Reaction notes
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