2-(Tributylstannyl)pyridine → HCID 136401541, compound
Reaction equation
[CH2:1]([O:3][C:4]([C:6]1[C:7]([OH:22])=[C:8]2[C:15]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)=[N:14][O:13][C:9]2=[C:10](Br)[N:11]=1)=[O:5])[CH3:2].CCCC[Sn]([C:36]1[N:41]=[CH:40][CH:39]=[CH:38][CH:37]=1)(CCCC)CCCC>>[CH2:1]([O:3][C:4]([C:6]1[C:7]([OH:22])=[C:8]2[C:15]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)=[N:14][O:13][C:9]2=[C:10]([C:40]2[CH:39]=[CH:38][CH:37]=[CH:36][N:41]=2)[N:11]=1)=[O:5])[CH3:2]Participants
3
Procedure
Prepared in analogy to that of Example 12 from 7-Bromo-4-hydroxy-3-phenyl-isoxazolo[5,4-c]pyridine-5-carboxylic acid ethyl ester and 2-(1,1,1-tributylstannyl)pyridine; ESI MS (m/z): 362.31 (M+H+); 360.34 (M−H+).
Sources & evidence
- ORD record
- ord-3cc02755af0648fba373befcc63f15b9
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08269008B2
Reaction notes
Loading…