1H-Indole-4-boronic acid, pinacol ester → HCID 59151293, compound
Reaction equation
[CH2:1]([N:8]([CH:13]1[CH2:18][CH2:17][N:16]([CH2:19][C:20]2[S:28][C:27]3[C:26]([N:29]4[CH2:34][CH2:33][O:32][CH2:31][CH2:30]4)=[N:25][C:24](Cl)=[N:23][C:22]=3[CH:21]=2)[CH2:15][CH2:14]1)[CH2:9][CH2:10][O:11][CH3:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CC1(C)C(C)(C)OB([C:44]2[CH:52]=[CH:51][CH:50]=[C:49]3[C:45]=2[CH:46]=[CH:47][NH:48]3)O1>>[CH2:1]([N:8]([CH:13]1[CH2:18][CH2:17][N:16]([CH2:19][C:20]2[S:28][C:27]3[C:26]([N:29]4[CH2:34][CH2:33][O:32][CH2:31][CH2:30]4)=[N:25][C:24]([C:44]4[CH:52]=[CH:51][CH:50]=[C:49]5[C:45]=4[CH:46]=[CH:47][NH:48]5)=[N:23][C:22]=3[CH:21]=2)[CH2:15][CH2:14]1)[CH2:9][CH2:10][O:11][CH3:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
3
Procedure
Benzyl-[1-(2-chloro-4-morpholin-4-yl-thieno[3,2-d]pyrimidine-6-ylmethyl)-piperidin-4-yl]-(2-methoxy-ethyl)-amine (150 mg), was used in a Suzuki coupling with 4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-indole (141 mg), to give after flash silica purification the title compound (105 mg) as a white solid.
Workup
- customto give
- customafter flash silica purification the title compound (105 mg) as a white solid
Sources & evidence
- ORD record
- ord-8f11d79e368848a58781c0eee39bfe2a
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08252792B2
Reaction notes
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