HCID 178516960, compound → 3-Bromo-5-chloro-benzofuro[3,2-c]isoquinoline
Reaction equation
O[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([Br:12])[CH:10]=2)[C:5]2[O:13][C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=3[C:4]=2[N:3]=1.[Cl:20]C1C=C2C(C3OC4C=CC=CC=4C=3N=C2O)=CC=1>>[Br:12][C:9]1[CH:10]=[C:11]2[C:6]([C:5]3[O:13][C:14]4[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=4[C:4]=3[N:3]=[C:2]2[Cl:20])=[CH:7][CH:8]=1Participants
3
Procedure
The procedure was similar to step S19C, while the starting material was 20B in stead of 19B.
Sources & evidence
- ORD record
- ord-8eae5916025c4278845ff1aafc68502b
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08969373B2
Reaction notes
Loading…