Hydrochloric Acid → HCID 18422308, compound
Reaction equation
CC(C)([O-])C.[K+].[NH2:7][C:8]1[CH:28]=[CH:27][CH:26]=[CH:25][C:9]=1[NH:10][C:11]1[S:15][C:14]2[CH:16]=[CH:17][CH:18]=[CH:19][C:13]=2[C:12]=1[C:20](OCC)=[O:21].Cl>COCCOC>[CH:19]1[C:13]2[C:12]3[C:20](=[O:21])[NH:7][C:8]4[CH:28]=[CH:27][CH:26]=[CH:25][C:9]=4[NH:10][C:11]=3[S:15][C:14]=2[CH:16]=[CH:17][CH:18]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Potassium tert-butoxide (718 mg) was suspended in 1,2-dimethoxyethane (35 ml) and the mixture was refluxed under heating. Thereto was added dropwise ethyl 2-(2-aminoanilino)benzo[b]thiophene-3-carboxylate (1.0 g) dissolved in 1,2-dimethoxyethane (35 ml) over 15 minutes. After 30 minutes, potassium tert-butoxide (359 mg) was added and the mixture was refluxed under heating for 1 hour. After the completion of the reaction, the reaction mixture was allowed to cool to room temperature and poured into 0.5N hydrochloric acid. The mixed solution was extracted 3 times with chloroform, and washed with water and dried over magnesium sulfate. The solution was filtered and the solvent was evaporated under reduced pressure. The precipitated crude crystals were washed with ethyl acetate and diisopropyl ether to give 6H-[1]benzothieno[2,3-b][1,5]benzodiazepin-12(11H)-one (300 mg).
Workup
- temperaturethe mixture was refluxed
- temperatureunder heating
- temperaturethe mixture was refluxed
- temperatureunder heating for 1 hour
- customAfter the completion of the reaction
- extractionThe mixed solution was extracted 3 times with chloroform
- washwashed with water
- dry with materialdried over magnesium sulfate
- filtrationThe solution was filtered
- customthe solvent was evaporated under reduced pressure
- customThe precipitated crude crystals
- washwere washed with ethyl acetate and diisopropyl ether
Sources & evidence
- ORD record
- ord-b380e102c7bb43668f8fe2054d45a34d
- Source dataset
- uspto-grants-2001_08
- Patent number
- US06271225B1
Reaction notes
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