Methylamine → HCID 57856004, compound
Reaction equation
[Cl:1][C:2]1[C:3]2[C:8]([CH:9]=[C:10]3[C:15]=1[N:14]=[C:13]([C:16]1[N:17]([C:25]4[C:30]([Cl:31])=[CH:29][CH:28]=[CH:27][N:26]=4)[N:18]=[C:19]([C:21]([F:24])([F:23])[F:22])[CH:20]=1)[O:12][C:11]3=[O:32])=[N:7][C:6]([C:33]([F:36])([F:35])[F:34])=[CH:5][CH:4]=2.[CH3:37][NH2:38]>C1COCC1>[CH3:37][NH:38][C:11]([C:10]1[CH:9]=[C:8]2[C:3]([CH:4]=[CH:5][C:6]([C:33]([F:35])([F:34])[F:36])=[N:7]2)=[C:2]([Cl:1])[C:15]=1[NH:14][C:13]([C:16]1[N:17]([C:25]2[C:30]([Cl:31])=[CH:29][CH:28]=[CH:27][N:26]=2)[N:18]=[C:19]([C:21]([F:22])([F:24])[F:23])[CH:20]=1)=[O:12])=[O:32]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
9-Chloro-2-[2-(3-chloro-pyridin-2-yl)-5-trifluoromethyl-2H-pyrazol-3-yl]-6-trifluoromethyl-3-oxa-1,5-diaza-anthracen-4-one is reacted with methylamine in THF analogously to the procedure given in step i) of example H-18. The title product is obtained as yellow crystals after flash column chromatography eluting with 1:1 hexane:ethyl acetate. m.p.: 235-237° C.
Sources & evidence
- ORD record
- ord-85a77e43d361455c9aaa9329abfc809f
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08580785B2
Reaction notes
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