(2,3-Dihydro-1,4-benzodioxin-6-yl)boronic acid → HCID 86721264, compound
Reaction equation
Br[C:2]1[N:6]([C:7]([CH3:10])([CH3:9])[CH3:8])[N:5]=[CH:4][C:3]=1[C:11]1[S:12][CH:13]=[C:14]([CH2:16][C:17]([NH:19][CH2:20][CH:21]2[CH2:26][CH2:25][O:24][CH2:23][CH2:22]2)=[O:18])[N:15]=1.[O:27]1[CH2:32][CH2:31][O:30][C:29]2[CH:33]=[C:34](B(O)O)[CH:35]=[CH:36][C:28]1=2>>[C:7]([N:6]1[C:2]([C:34]2[CH:35]=[CH:36][C:28]3[O:27][CH2:32][CH2:31][O:30][C:29]=3[CH:33]=2)=[C:3]([C:11]2[S:12][CH:13]=[C:14]([CH2:16][C:17]([NH:19][CH2:20][CH:21]3[CH2:26][CH2:25][O:24][CH2:23][CH2:22]3)=[O:18])[N:15]=2)[CH:4]=[N:5]1)([CH3:10])([CH3:9])[CH3:8]Participants
3
Procedure
Using 2-(2-(5-bromo-1-tert-butyl-1H-pyrazol-4-yl)thiazol-4-yl)-N-((tetrahydro-2H-pyran-4-yl)methyl)acetamide and (2,3-dihydrobenzo[b][1,4]dioxin-6-yl)boronic acid and by reaction and purification in the same manner as in the method described in Example 43, the title compound was obtained.
Workup
- customby reaction and purification in the same manner as in the method
Sources & evidence
- ORD record
- ord-5ef7fddcf0444bf9ac9e7138a84b357c
- Source dataset
- uspto-grants-2015_10
- Patent number
- US09156837B2
Reaction notes
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