HCID 178488258, compound → HCID 86722281, compound

Reaction equation

O[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([Cl:12])[CH:10]=2)[C:5]2[O:13][C:14]3[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][C:15]=3[C:4]=2[N:3]=1.[Cl:22]C1C=C2C(C3OC4C=CC=CC=4C=3N=C2O)=CC=1>>[Cl:12][C:9]1[CH:10]=[C:11]2[C:6]([C:5]3[O:13][C:14]4[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][C:15]=4[C:4]=3[N:3]=[C:2]2[Cl:22])=[CH:7][CH:8]=1

Participants

Reactant 2

HCID 178488258HCID 178488258, compound

HCID 1785169623-Chloro-benzofuro[3,2-c]isoquinoline-5-ol

Product 1

HCID 86722281HCID 86722281, compound

Procedure

The procedure was similar to step S19C, while the starting material was 26B in stead of 19B.

Sources & evidence

ORD record: ord-3d29e769574e4a4295a18cf80fc508a8
Source dataset: uspto-grants-2015_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08969373B2

Reaction notes

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