Ethanol → HCID 178434443, compound
Reaction equation
C([O-])(=O)C.[Na+].[NH2:6][NH:7][C:8]([NH2:10])=[S:9].C(O)C.[CH3:14][C:15]1[C:23]2[C:18](=[N:19][CH:20]=[C:21]([CH:24]=O)[CH:22]=2)[NH:17][N:16]=1>O>[CH3:14][C:15]1[C:23]2[C:18](=[N:19][CH:20]=[C:21]([CH:24]=[N:6][NH:7][C:8]([NH2:10])=[S:9])[CH:22]=2)[NH:17][N:16]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 80 °C
Procedure
Sodium acetate (166 mg, 2.02 mmol), thiosemicarbazide (333 mg, 3.66 mmol), 100 ml ethanol and 2 ml distilled water were charged into a 250 ml round bottom flask. The resulting suspension was heated to 80° C. until it becomes a clear solution. The reaction was then cooled down to room temperature and the resulting mixture was added into a 250 ml round bottom flask containing 3-methyl-1H-pyrazolo[3,4-b]pyridine-5-carbaldehyde (333 mg, 2.1 mmol). After the addition, the resulting mixture was heated to 80° C. for 16 hours. The mixture was cooled to room temperature and solid was precipitated out. The solid was filtered off and washed with ether (50 ml). The product (500 mg, y=95%) was used directly for the next step without further purification.
Workup
- additionwere charged into a 250 ml round bottom flask
- temperatureThe reaction was then cooled down to room temperature
- additionthe resulting mixture was added into a 250 ml round bottom flask
- additionAfter the addition
- temperaturethe resulting mixture was heated to 80° C. for 16 hours
- temperatureThe mixture was cooled to room temperature
- customsolid was precipitated out
- filtrationThe solid was filtered off
- washwashed with ether (50 ml)
- customThe product (500 mg, y=95%) was used directly for the next step without further purification
Sources & evidence
- ORD record
- ord-e20d695cea87441f8cdc6f03f778d7b3
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07354944B2
Reaction notes
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