Ethanol → HCID 10133536, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=C([CH:7]=[CH:8][C:9]=1[C:10]([N:12]1[C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][C:17]=2[CH2:16][N:15]2[CH:23]=[CH:24][CH:25]=[C:14]2[CH2:13]1)=[O:11])C#N.[OH-:26].[Na+].[CH2:28]([OH:30])[CH3:29]>>[Cl:1][C:2]1[CH:3]=[C:29]([CH:7]=[CH:8][C:9]=1[C:10]([N:12]1[C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][C:17]=2[CH2:16][N:15]2[CH:23]=[CH:24][CH:25]=[C:14]2[CH2:13]1)=[O:11])[C:28]([OH:26])=[O:30]Participants
Procedure
To a suspension of 3-chloro-4-(5H,11H-pyrrolo-[2,1-c][1.4]-benzodiazepine-10-carbonyl)-benzonitrile (90.72 g) in ethanol was added 10 N sodium hydroxide (1.02 ml) and the mixture heated under reflux for two hours. The solvent was removed in vacuo, the residue dissolved in water, and made acidic with 2 N hydrochloric acid (4.7 ml). The resulting precipitate was extracted with ethyl acetate, and the organic phase dried over anhydrous sodium sulfate. After removing the solvent in vacuo, a foam was triturated with diethyl ether for 18 hours and filtered to give a crude product (0.69 g). The crude product was purified by treatment with activated charcoal in methanol. Crystallization from methanol/ether afforded the title compound as a purified solid (0.29 g), m.p. 198-199° C.; MS (EI), m/z: 366 (M)+.
Workup
- temperaturethe mixture heated
- temperatureunder reflux for two hours
- customThe solvent was removed in vacuo
- dissolutionthe residue dissolved in water
- extractionThe resulting precipitate was extracted with ethyl acetate
- dry with materialthe organic phase dried over anhydrous sodium sulfate
- customAfter removing the solvent in vacuo
- customa foam was triturated with diethyl ether for 18 hours
- filtrationfiltered
- customto give a crude product (0.69 g)
- customThe crude product was purified by treatment with activated charcoal in methanol
- customCrystallization from methanol/ether
Sources & evidence
- ORD record
- ord-6e8552cee4e547c0b333960321698237
- Source dataset
- uspto-grants-2004_12
- Patent number
- US06831079B1
Reaction notes
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