6-Ethyl-3,5-dimethoxy-pyridine-2-carboxylic acid hydrazide → N[6-ethyl-3,5-dimethoxy-pyridine-2-carboxamidyl]-N'-(1-Methyl-1H-indol-5-yl)-thiourea
Reaction equation
[CH2:1]([C:3]1[N:8]=[C:7]([C:9]([NH:11][NH2:12])=[O:10])[C:6]([O:13][CH3:14])=[CH:5][C:4]=1[O:15][CH3:16])[CH3:2].[N:17]([C:20]1[CH:21]=[C:22]2[C:26](=[CH:27][CH:28]=1)[N:25]([CH3:29])[CH:24]=[CH:23]2)=[C:18]=[S:19]>C(O)C>[CH2:1]([C:3]1[N:8]=[C:7]([C:9]([NH:11][NH:12][C:18]([NH:17][C:20]2[CH:21]=[C:22]3[C:26](=[CH:27][CH:28]=2)[N:25]([CH3:29])[CH:24]=[CH:23]3)=[S:19])=[O:10])[C:6]([O:13][CH3:14])=[CH:5][C:4]=1[O:15][CH3:16])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A flask was charged with 6-ethyl-3,5-dimethoxy-pyridine-2-carboxylic acid hydrazide (34 mg; 0.15 mmol), 5-isothiocyanato-1-methyl-1H-indole (28 mg; 0.15 mmol) and ethanol (2 mL) and the mixture was heated at reflux for three hours. The reaction was then cooled, and the precipitate was filtered and dried to give N-[6-Ethyl-3,5-dimethoxy-pyridine-2-carboxamidyl]-N′-(1-Methyl-1H-indol-5-yl)-thiourea (44 mg; 0.11 mmol).
Workup
- temperaturethe mixture was heated
- temperatureat reflux for three hours
- temperatureThe reaction was then cooled
- filtrationthe precipitate was filtered
- customdried
Sources & evidence
- ORD record
- ord-6c084e9589104982b1407c99756893ed
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09206162B2
Reaction notes
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