2-Iodobenzaldehyde → HCID 21099432, compound
Reaction equation
I[C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=[O:5].[F:10][C:11]1[CH:16]=[C:15]([F:17])[CH:14]=[CH:13][C:12]=1[CH2:18][CH2:19][C:20]1[CH:25]=[CH:24][C:23]([S:26](C2C=CC=CC=2)(=[O:28])=[O:27])=[CH:22][CH:21]=1>>[F:10][C:11]1[CH:16]=[C:15]([F:17])[CH:14]=[CH:13][C:12]=1/[CH:18]=[CH:19]/[C:20]1[CH:25]=[CH:24][C:23]([S:26]([C:2]2[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=2[CH:4]=[O:5])(=[O:28])=[O:27])=[CH:22][CH:21]=1Participants
3
Procedure
2-({4-[(E)-2-(2,4-difluorophenyl)vinyl]phenyl}sulfonyl)benzaldehyde was prepared according to the method of Example 135, Step 2 using 2-iodobenzaldehyde in place of (S)-1-(2-iodophenyl)ethanol and Intermediate 2 in place of Intermediate 1.
Sources & evidence
- ORD record
- ord-72a14ffdce794505b1471c52a21997a2
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07217740B2
Reaction notes
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