2-Cyclopropylethan-1-ol → 4-[2-(2-Cyclopropylethoxy)-4-fluorophenyl]-N-{3-[(methylsulfonyl)methyl]phenyl}-1,3,5-triazin-2-amine
Reaction equation
F[C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C:9]1[N:14]=[CH:13][N:12]=[C:11]([NH:15][C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([CH2:22][S:23]([CH3:26])(=[O:25])=[O:24])[CH:17]=2)[N:10]=1.[CH:27]1([CH2:30][CH2:31][OH:32])[CH2:29][CH2:28]1>>[CH:27]1([CH2:30][CH2:31][O:32][C:2]2[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=2[C:9]2[N:14]=[CH:13][N:12]=[C:11]([NH:15][C:16]3[CH:21]=[CH:20][CH:19]=[C:18]([CH2:22][S:23]([CH3:26])(=[O:25])=[O:24])[CH:17]=3)[N:10]=2)[CH2:29][CH2:28]1Participants
3
Procedure
Starting with 4-(2,4-difluorophenyl)-N-{3-[(methylsulfonyl)methyl]phenyl}-1,3,5-triazin-2-amine (75 mg; 0.19 mmol), intermediate 42.1, and 2-cyclopropylethanol (46.2 mg; 0.773 mmol), example 48 was prepared analogously to the procedure for the preparation of example 42.
Workup
- customwas prepared analogously to the procedure for the preparation of example 42
Sources & evidence
- ORD record
- ord-d1e416d0bf1448748a48b7d46f57c2f0
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08916557B2
Reaction notes
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