Furan-3-boronic acid → Ethyl 6-(furan-3-yl)imidazo[1,2-a]pyridine-2-carboxylate
Reaction equation
C([Si](C(C)C)(C(C)C)N1[CH:9]=[CH:8][C:7]([C:10]2[CH:11]=[CH:12][C:13]3[N:14]([CH:16]=[C:17]([C:19]([O:21][CH2:22][CH3:23])=[O:20])[N:18]=3)[CH:15]=2)=[CH:6]1)(C)C.[O:30]1C=CC(B(O)O)=C1>>[O:30]1[CH:9]=[CH:8][C:7]([C:10]2[CH:11]=[CH:12][C:13]3[N:14]([CH:16]=[C:17]([C:19]([O:21][CH2:22][CH3:23])=[O:20])[N:18]=3)[CH:15]=2)=[CH:6]1Participants
3
Procedure
This product is prepared under conditions similar to those described for the preparation of Intermediate 15 (step 15.1), replacing the 1-(triisopropylsilyl)pyrrole-3-boronic acid with furan-3-boronic acid.
Workup
- customThis product is prepared under conditions similar to
Sources & evidence
- ORD record
- ord-604cfe8d9b9c48aa80fcb3b078e5d3fe
- Source dataset
- uspto-grants-2012_11
- Patent number
- US08314109B2
Reaction notes
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