4-Fluoro-3-methoxybenzaldehyde → HCID 22714661, compound
Reaction equation
[CH3:1][S:2]([C:4]1[CH:10]=[CH:9][C:7]([NH2:8])=[CH:6][CH:5]=1)=[O:3].[F:11][C:12]1[CH:19]=[CH:18][C:15]([CH:16]=O)=[CH:14][C:13]=1[O:20][CH3:21]>>[F:11][C:12]1[CH:19]=[CH:18][C:15]([CH:16]=[N:8][C:7]2[CH:9]=[CH:10][C:4]([S:2]([CH3:1])=[O:3])=[CH:5][CH:6]=2)=[CH:14][C:13]=1[O:20][CH3:21]Participants
3
Procedure
Following a similar procedure to that described in section a of example 1, but starting from 4-methylsulfinylaniline (obtained in reference example 2) instead of 4-methylsulfonylaniline and from 4-fluoro-3-methoxybenzaldehyde instead of 4-isopropoxybenzaldehyde, the desired compound was obtained, which was directly used in the next step.
Sources & evidence
- ORD record
- ord-44ce878267544bcaaefb565f16cccd39
- Source dataset
- uspto-grants-2004_06
- Patent number
- US06743816B2
Reaction notes
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