Sodium Bicarbonate → HCID 21460702, compound
Reaction equation
[N+:1]([C:4]1[CH:29]=[CH:28][C:7]([C:8](=[O:27])[CH2:9][NH:10][C:11]2[C:19]3[C:14](=[CH:15][C:16]([Cl:21])=[CH:17][C:18]=3[Cl:20])[NH:13][C:12]=2[C:22]([O:24][CH2:25][CH3:26])=[O:23])=[CH:6][CH:5]=1)([O-])=O.O.[Sn](Cl)Cl.C(OCC)(=O)C.O.C(=O)([O-])O.[Na+]>C(O)C>[NH2:1][C:4]1[CH:29]=[CH:28][C:7]([C:8](=[O:27])[CH2:9][NH:10][C:11]2[C:19]3[C:14](=[CH:15][C:16]([Cl:21])=[CH:17][C:18]=3[Cl:20])[NH:13][C:12]=2[C:22]([O:24][CH2:25][CH3:26])=[O:23])=[CH:6][CH:5]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 70 °C
Procedure
Dissolve 3-[(4-nitrophenacyl)amino]-2-carbethoxy-4,6-dichloroindole (0.5 g, 1.184 mmol) in ethanol (20 mL) and tin (II) chloride monohydrate (1.06 g, 7.1 mmol). Heat to 70° C. overnight. Pour into ethyl acetate/water (200 mL) and add solid sodium hydrogen carbonate to obtain pH 7. Filter and evaporate the solvent in vacuo to give the title compound as a pale yellow oil (0.477, 100%).
Workup
- customto obtain pH 7
- filtrationFilter
- customevaporate the solvent in vacuo
Sources & evidence
- ORD record
- ord-edcbd6f90f0c46f792f55b97bdaa9952
- Source dataset
- uspto-grants-1993_02
- Patent number
- US05189054
Reaction notes
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