6-Chloro-7-methylimidazo[1,2-b]pyridazine → HCID 21800330, compound

HRID 2395967Notes

Reaction equation

HRID 2395967 reaction equation
[Cl:1][C:2]1[C:3]([CH3:11])=[CH:4][C:5]2[N:6]([CH:8]=[CH:9][N:10]=2)[N:7]=1.CN(C=[N:16][S:17]([CH2:20][CH:21]([CH:24]([CH3:26])[CH3:25])[CH2:22][OH:23])(=[O:19])=[O:18])C>>[ClH:1].[CH:24]([CH:21]([CH2:20][S:17](=[O:19])(=[O:18])[NH2:16])[CH2:22][O:23][C:2]1[C:3]([CH3:11])=[CH:4][C:5]2[N:6]([CH:8]=[CH:9][N:10]=2)[N:7]=1)([CH3:26])[CH3:25]

Participants

3

Reactant 2

HCID 122483366-Chloro-7-methylimidazo[1,2-b]pyridazineHCID 53813453HCID 53813453, compound

Product 1

HCID 21800330HCID 21800330, compound

Procedure

Using 0.8 g of 6-chloro-7-methylimidazo[1,2-b]pyridazine and 1.29 g of 3-(N,N-dimethylaminomethylene)aminosulfonyl-2-isopropyl-1-propanol, 1.37 gof the title compound was obtained in the same manner as in Examples 14 and

Sources & evidence

ORD record
ord-736f8dd41b2f43819df0cab870809374
Source dataset
uspto-grants-1996_02
Patent number
US05491145

Reaction notes

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