Reaction equation
C[N:2]1[CH2:8][CH2:7][CH2:6][N:5]([C:9]2[N:13]([CH2:14][CH2:15][O:16][CH2:17][CH3:18])[C:12]3[CH:19]=[CH:20][CH:21]=[CH:22][C:11]=3[N:10]=2)[CH2:4][CH2:3]1.Cl[C:24]([O:26][CH2:27][CH3:28])=[O:25]>C1(C)C=CC=CC=1.C(OCC)(=O)C>[CH2:27]([O:26][C:24]([N:2]1[CH2:8][CH2:7][CH2:6][N:5]([C:9]2[N:13]([CH2:14][CH2:15][O:16][CH2:17][CH3:18])[C:12]3[CH:19]=[CH:20][CH:21]=[CH:22][C:11]=3[N:10]=2)[CH2:4][CH2:3]1)=[O:25])[CH3:28]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 80 °C
Procedure
Combine 1-methyl-4-(1-(2-ethoxyethyl)-1H-benzimidazol-2-yl)[1,4]diazepane (1.79 g, 5.9 mmol) and ethyl chloroformate (0.75 mL, 7.8 mmol) in toluene (20 mL). Heat to 80° C. After 2 hours, cool the reaction mixture and dilute with ethyl acetate. Extract with a saturated aqueous sodium bicarbonate solution, dry the organic layer over MgSO4, filter, and evaporate in vacuo to give 1-ethoxycarbonyl-4-(1-(2-ethoxyethyl)-1H-benzimidazol-2-yl)[1,4]diazepane: Rf =0.87 (silica gel, dichloromethane/methanol, 90/10). Combine 1-ethoxycarbonyl-4-(1-(2-ethoxyethyl)-1H-benzimidazol-2-yl)[1,4]diazepane (17.2 g, 47.6 mmol), hydrazine hydrate (40 mL), and potassium hydroxide (40.7 g, 725 mmol) in ethylene glycol (150 mL). Heat to reflux. After 5 hours, cool the reaction mixture and dilute with water (500 mL). Extract three times with dichloromethane. Combine the dichloromethane layers and extract with a saturated aqueous sodium bicarbonate solution and then brine. Dry the organic layer over MgSO4, filter, and evaporate in vacuo to give the title compound: Rf =0.25 (silica gel, dichloromethane/methanol, 90/10).
Workup
- temperaturecool the reaction mixture
- extractionExtract with a saturated aqueous sodium bicarbonate solution
- dry with materialdry the organic layer over MgSO4
- filtrationfilter
- customevaporate in vacuo
Sources & evidence
- ORD record
- ord-131926130f2a4137973af6d85c1b175c
- Source dataset
- uspto-grants-1999_08
- Patent number
- US05932571
Linked notes
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