8-Methoxy-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile → 8-Hydroxy-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile
Reaction equation
C[O:2][C:3]1[CH:4]=[CH:5][C:6]2[C:18](=[O:19])[C:17]3[C:16]4[C:11](=[CH:12][C:13]([C:20]#[N:21])=[CH:14][CH:15]=4)[NH:10][C:9]=3[C:8]([CH3:23])([CH3:22])[C:7]=2[CH:24]=1>Cl.N1C=CC=CC=1>[OH:2][C:3]1[CH:4]=[CH:5][C:6]2[C:18](=[O:19])[C:17]3[C:16]4[C:11](=[CH:12][C:13]([C:20]#[N:21])=[CH:14][CH:15]=4)[NH:10][C:9]=3[C:8]([CH3:22])([CH3:23])[C:7]=2[CH:24]=1Participants
Conditions
- Temperature
- 170 °C
Procedure
8-Methoxy-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile (Compound A5-2, 6.58 g, 20.8 mmol) was dissolved in pyridine hydrochloric acid salt (25.0 g), and stirred at 170° C. for 13 hours. The reaction mixture was partitioned in ethyl acetate (400 mL) and distilled water (400 mL), and the aqueous layer was extracted one more time with ethyl acetate (400 mL). The combined organic layer was washed twice with distilled water (100 mL) and once with saturated brine (100 mL) in order, and dried over anhydrous sodium sulfate. The organic layer was concentrated under reduced pressure to yield a product, which was suspended and washed with a small amount of CPME to obtain the title compound as a colorless crystal (5.91 g, 93%).
Workup
- customThe reaction mixture was partitioned in ethyl acetate (400 mL)
- distillationdistilled water (400 mL)
- extractionthe aqueous layer was extracted one more time with ethyl acetate (400 mL)
- washThe combined organic layer was washed twice with distilled water (100 mL) and once with saturated brine (100 mL) in order
- dry with materialdried over anhydrous sodium sulfate
- concentrationThe organic layer was concentrated under reduced pressure
- customto yield a product, which
- washwashed with a small amount of CPME
Sources & evidence
- ORD record
- ord-d8561717c7d74bdf9a16ca373b103e59
- Source dataset
- uspto-grants-2016_06
- Patent number
- US09365514B2
Reaction notes
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