Thiophene-3-boronic acid → HCID 53670022, compound
Reaction equation
Br[C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[CH:7][N:8]2[CH2:11][C@@H:12]2[CH2:16][CH2:15][CH2:14][N:13]2[CH3:17])=[CH:4][CH:3]=1.[S:18]1[CH:22]=[CH:21][C:20](B(O)O)=[CH:19]1>>[CH3:17][N:13]1[CH2:14][CH2:15][CH2:16][C@@H:12]1[CH2:11][N:8]1[C:9]2[C:5](=[CH:4][CH:3]=[C:2]([C:20]3[CH:21]=[CH:22][S:18][CH:19]=3)[CH:10]=2)[CH:6]=[CH:7]1Participants
3
Procedure
(39.9 mg, 79%); from (S)-6-bromo-1-((N-methylpyrrolidin-2-yl)methyl)indole (50.0 mg, 0.17 mmol) and thiophene-3-boronic acid (43.6 mg, 0.34 mmol).
Sources & evidence
- ORD record
- ord-a5a20ef77ca14a8d8f4d29cb72f323d0
- Source dataset
- uspto-grants-2003_10
- Patent number
- US06635639B2
Reaction notes
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