4-Hydroxy-3,3-dimethyl-1-butanesulfonamide → 1-Butanesulfonamide, 3,3-dimethyl-4-((7-methyl(1,2,4)triazolo(1,5-b)pyridazin-6-yl)oxy)-

HRID 274270

反応式

HRID 274270 の反応式
[OH:1][CH2:2][C:3]([CH3:11])([CH3:10])[CH2:4][CH2:5][S:6]([NH2:9])(=[O:8])=[O:7].Cl[C:13]1[C:14]([CH3:22])=[CH:15][C:16]2[N:17]([N:19]=[CH:20][N:21]=2)[N:18]=1>>[CH3:10][C:3]([CH3:11])([CH2:4][CH2:5][S:6](=[O:7])(=[O:8])[NH2:9])[CH2:2][O:1][C:13]1[C:14]([CH3:22])=[CH:15][C:16]2[N:17]([N:19]=[CH:20][N:21]=2)[N:18]=1

参加物

3

反応物 2

HCID 107499174-Hydroxy-3,3-dimethyl-1-butanesulfonamideHCID 118051586-Chloro-7-methyl-[1,2,4]triazolo[1,5-b]pyridazine

生成物 1

HCID 30737871-Butanesulfonamide, 3,3-dimethyl-4-((7-methyl(1,2,4)triazolo(1,5-b)pyridazin-6-yl)oxy)-

実験手順

Using 4-hydroxy-3,3-dimethyl-1-butanesulfonamide and 6-chloro-7-methyl[1,2,4]triazolo[1,5-b]pyridazine, the same reaction was conducted as in Example 5 to produce the title compound. m.p. 214°-215° C.

後処理

  1. customthe same reaction

出典と根拠

ORDレコード
ord-7c838acca3f743f9aeb4a753d5e38f1e
出典データセット
uspto-grants-1995_02
特許番号
US05389633

関連ノート

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