Benzaldehyde → HCID 22335575, compound
Reaction equation
[NH2:1][C:2]1[CH:6]=[CH:5][NH:4][N:3]=1.[C:7]([N+:11]#[C-:12])([CH3:10])([CH3:9])[CH3:8].[CH:13](=O)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>Cl(O)(=O)(=O)=O>[C:7]([NH:11][C:12]1[N:3]2[NH:4][CH:5]=[CH:6][C:2]2=[N:1][C:13]=1[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)([CH3:10])([CH3:9])[CH3:8]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Compound 24 was prepared in accordance with the general synthesis instructions from 1.0 ml (0.1 mmol) 3-amino-pyrazole solution (0.1 M, MC), 0.575 ml (0.115 mmol) tert-butylisonitrile solution (0.2 M, MC), 0.500 ml (0.15 mmol) benzaldehyde solution (0.3 M, MC) and 10 μl perchloric acid (w=20%) in a substance library.
Sources & evidence
- ORD record
- ord-c3ac994a8d64435e8f83a934e8734a2c
- Source dataset
- uspto-grants-2003_12
- Patent number
- US06657064B2
Reaction notes
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