2-(Trifluoromethoxy)phenylboronic Acid (contains varying amounts of Anhydride) → HCID 66576282, compound
Reaction equation
Cl[C:2]1[N:7]=[CH:6][N:5]=[C:4]([NH:8][C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([CH2:15][S:16]([CH3:19])(=[O:18])=[O:17])[CH:10]=2)[N:3]=1.[F:20][C:21]([F:33])([F:32])[O:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=1B(O)O>>[CH3:19][S:16]([CH2:15][C:11]1[CH:10]=[C:9]([NH:8][C:4]2[N:3]=[C:2]([C:24]3[CH:25]=[CH:26][CH:27]=[CH:28][C:23]=3[O:22][C:21]([F:20])([F:33])[F:32])[N:7]=[CH:6][N:5]=2)[CH:14]=[CH:13][CH:12]=1)(=[O:18])=[O:17]Participants
3
Procedure
Example 7 was prepared under similar conditions as described in the preparation of Example 1 using crude 4-chloro-N-{3-[(methylsulfonyl)methyl]phenyl}-1,3,5-triazin-2-amine and [2-(trifluoromethoxy)phenyl]boronic acid (ABCR GmbH & CO. KG). The batch was purified by preparative HPLC:
Workup
- customExample 7 was prepared under similar conditions
- customThe batch was purified by preparative HPLC
Sources & evidence
- ORD record
- ord-cd7a703154ae41b6adb96a19e885c9ac
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08916557B2
Reaction notes
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