2-Bromo-4'-(trifluoromethyl)acetophenone → HCID 2742458, compound
Reaction equation
Br[CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([C:11]([F:14])([F:13])[F:12])=[CH:7][CH:6]=1)=O.[C:15]([CH2:17][C:18]([NH2:20])=[S:19])#[N:16]>>[F:12][C:11]([F:14])([F:13])[C:8]1[CH:9]=[CH:10][C:5]([C:3]2[N:20]=[C:18]([CH2:17][C:15]#[N:16])[S:19][CH:2]=2)=[CH:6][CH:7]=1Participants
3
Procedure
This compound was synthesized from 2-bromo-1-(4-(trifluoromethyl)phenyl)ethanone and 2-cyanothioacetamide as described in example 1 step 1 (2.4 g, 48% yield), and it was carried through without further purification. MS (ESI) m/z: Calculated for C12H7F3N2S: 268.03. found: 269.0 (M+H)+.
Workup
- customwas carried through without further purification
Sources & evidence
- ORD record
- ord-7e5d1bda92664ea1a5f4accf8ea32e89
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08901156B2
Reaction notes
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