Ethanol → HCID 13134784, compound
Reaction equation
O=[C:2]1[CH2:8][C:7]2[CH:9]=[CH:10][CH:11]=[N:12][C:6]=2[S:5][C:4]2[CH:13]=[CH:14][C:15]([CH2:17][C:18]([OH:20])=[O:19])=[CH:16][C:3]1=2.O.NN.C(O)C.[OH-].[Na+]>C(O)(=O)C.C(O)COCCO>[N:12]1[C:6]2[S:5][C:4]3[CH:13]=[CH:14][C:15]([CH2:17][C:18]([OH:20])=[O:19])=[CH:16][C:3]=3[CH2:2][CH2:8][C:7]=2[CH:9]=[CH:10][CH:11]=1Participants
Conditions
- Temperature
- 135 °C
Procedure
A mixture of 400 mg of (5,6-dihydro-6-oxo benzo[b]pyrido[3,2-f]-thiepin-8-yl)-acetic acid, 800 mg of hydrazine hydrate and 30 ml of ethanol was refluxed for 3 hours. The solvent was distilled off to obtain a solid substance, to which were added 1 g of sodium hydroxide and 8 ml of diethylene glycol, and the mixture was stirred under a nitrogen atmosphere at 135° C. for 1.5 hours. After cooling, ice water was added to the mixture, and the resulting mixture was acidified with acetic acid and extracted with chloroform. The extract was washed with water and dried over anhydrous sodium sulfate. The solvent was removed by distillation to obtain an oil, which was chromatographed over silica gel and eluted with chloroform ethanol (100/1) to obtain a power. This was recrystallized from 290 mg (yield: 76%) of (5,6-dihydro benzo[b]pyrido[3,2-f]thiepin-8-yl)-acetic acid as colorless needle crystals.
Workup
- temperaturewas refluxed for 3 hours
- distillationThe solvent was distilled off
- customto obtain a solid substance
- temperatureAfter cooling
- extractionextracted with chloroform
- washThe extract was washed with water
- dry with materialdried over anhydrous sodium sulfate
- customThe solvent was removed by distillation
- customto obtain an oil, which
- customwas chromatographed over silica gel
- washeluted with chloroform ethanol (100/1)
- customto obtain a power
Sources & evidence
- ORD record
- ord-bb216321d8b84d648da4c5d8a2ba1ab7
- Source dataset
- uspto-grants-1983_03
- Patent number
- US04377702
Reaction notes
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