Methanol → HCID 21107343, compound
Reaction equation
Br[C:2]1[CH:3]=[CH:4][C:5]2[NH:6][C:7]3[C:12]([C:13]=2[CH:14]=1)=[CH:11][CH:10]=[CH:9][CH:8]=3.[Cu][C:16]#[N:17].O.CO>CN1CCCC1=O>[CH:4]1[C:5]2[NH:6][C:7]3[C:12](=[CH:11][CH:10]=[CH:9][CH:8]=3)[C:13]=2[CH:14]=[C:2]([C:16]#[N:17])[CH:3]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 200 °C
Procedure
To a solution of 3-bromo-9H-carbazole (4.00 g, 16.3 mmol, 1 equiv) in N-Methyl-2-pyrrolidinone (40 mL) was added copper(I) cyanide (1.6012 g, 17.9 mmol, 1.1 equiv). The mixture was sealed and heated at 200° C. until TLC showed no starting material. The reaction solution was cooled and 60 mL of water was added. The off-white precipitate was filtered off and washed with EtOAc (3×20 mL). This filtrate was extracted with ethyl acetate (3×20 mL). The combined organic layers were washed with water (20 mL) and brine (20 mL), and then dried over Na2SO4. The solvent was removed under reduced pressure to afford red-brown oil. Methanol was added to the crude oil to afford 0.8251 g off-white precipitate as pure product. The mother liquid from the methanol precipitation was concentrated and purified by chromatography (25% EtOAc/Hex) to provide 0.28 g off-white solid. The combined yield was 35.5%.
Workup
- customThe mixture was sealed
- temperatureThe reaction solution was cooled
- filtrationThe off-white precipitate was filtered off
- washwashed with EtOAc (3×20 mL)
- extractionThis filtrate was extracted with ethyl acetate (3×20 mL)
- washThe combined organic layers were washed with water (20 mL) and brine (20 mL)
- dry with materialdried over Na2SO4
- customThe solvent was removed under reduced pressure
- customto afford red-brown oil
Sources & evidence
- ORD record
- ord-228734d63482442290bec5dea5e6c26f
- Source dataset
- uspto-grants-2014_11
- Patent number
- US08877797B2
Reaction notes
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