2-Tetralone → 3-Bromo-6,6-dimethyl-5,6-dihydro-benzo[b]carbazol-11-one
Reaction equation
[Br:1][C:2]1[CH:14]=[C:13]2[C:5]([C:6]3[C:7](=[O:23])[C:8]4[CH:20]=[CH:19][C:18](OC)=[CH:17][C:9]=4[C:10]([CH3:16])([CH3:15])[C:11]=3[NH:12]2)=[CH:4][CH:3]=1.C1C2C(=CC=CC=2)CCC1=O>>[Br:1][C:2]1[CH:14]=[C:13]2[C:5]([C:6]3[C:7](=[O:23])[C:8]4[CH:20]=[CH:19][CH:18]=[CH:17][C:9]=4[C:10]([CH3:15])([CH3:16])[C:11]=3[NH:12]2)=[CH:4][CH:3]=1Participants
3
Procedure
Under the same conditions as the method for synthesizing Compound A3-1 and Compound A4, the title compound was prepared from 3,4-dihydro-1H-naphthalen-2-one (560 mg).
Sources & evidence
- ORD record
- ord-2459270097e0446e9b145d6c2b1f6e22
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09126931B2
Reaction notes
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