Dimethylamine → HCID 21991546, compound
Reaction equation
C(OC(N1C[CH2:12][N:11]([C:14]2[C:15](=[O:33])[N:16]([CH2:29][CH:30]([CH3:32])[CH3:31])[N:17]=[C:18]([C:21]3[CH:26]=[CH:25][C:24](C)=[C:23](F)[CH:22]=3)[C:19]=2[CH3:20])[CH2:10]C1)=O)(C)(C)C.C1(CN2C(=O)C(C[O:46][S:47]([CH3:50])(=O)=[O:48])=CC(C3C=CC(S(C)(=O)=O)=CC=3)=N2)CC1.CNC>>[CH:30]1([CH2:29][N:16]2[C:15](=[O:33])[C:14]([N:11]([CH3:10])[CH3:12])=[C:19]([CH3:20])[C:18]([C:21]3[CH:22]=[CH:23][C:24]([S:47]([CH3:50])(=[O:48])=[O:46])=[CH:25][CH:26]=3)=[N:17]2)[CH2:31][CH2:32]1Participants
4
Reactant 3
Product 1
Procedure
Following the procedure of Example 1 (10), 2-cyclopropylmethyl-4-methanesulfonyloxymethyl-6-[4-(methyl-sulfonyl)phenyl]-2H-pyridazin-3-one and dimethylamine were reacted to yield the title compound as a yellow oil (yield: 65.6%).
Workup
- customwere reacted
Sources & evidence
- ORD record
- ord-51117be8824c445abd4949fe380f7aba
- Source dataset
- uspto-grants-2006_08
- Patent number
- US07087606B2
Reaction notes
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