m-Chloroperbenzoic acid → HCID 72700242, compound
Reaction equation
[CH:1]1([NH:4][C:5]([C:7]2[C:8](=[O:31])[C:9]3[CH:30]=[CH:29][CH:28]=[N:27][C:10]=3[N:11]([C:13]3[CH:18]=[CH:17][CH:16]=[C:15]([C:19]#[C:20][C:21]4[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=4)[CH:14]=3)[N:12]=2)=[O:6])[CH2:3][CH2:2]1.ClC1C=C(C=CC=1)C(OO)=[O:37]>ClCCl>[CH:1]1([NH:4][C:5]([C:7]2[C:8](=[O:31])[C:9]3[CH:30]=[CH:29][CH:28]=[N:27][C:10]=3[N:11]([C:13]3[CH:14]=[C:15]([C:19]#[C:20][C:21]4[CH:22]=[N+:23]([O-:37])[CH:24]=[CH:25][CH:26]=4)[CH:16]=[CH:17][CH:18]=3)[N:12]=2)=[O:6])[CH2:2][CH2:3]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
N-cyclopropyl-4-oxo-1-[3-(pyridin-3-ylethynyl)phenyl]-1,4-dihydropyridino[2,3-c]p yridazine-3-formamide (0.15 g, 0.36 mmol) was dissolved in 50 mL of dichloromethane solution, m-chloroperoxybenzoic acid (0.062 g, 0.36 mmol) was added and reacted at room temperature. After reaction was complete, separation was purified by liquid preparation chromatography column to obtain product 27 mg.
Workup
- customreacted at room temperature
- customAfter reaction
- customseparation
- customwas purified by liquid preparation chromatography column
Sources & evidence
- ORD record
- ord-e55733d5f6a541de9dd9d04466e70487
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09181244B1
Reaction notes
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