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6-Chloro-2,8-dimethyl[1,2,4]triazolo[1,5-b]pyridazine → 1-Butanesulfonamide, 2-(((2,8-dimethyl(1,2,4)triazolo(1,5-b)pyridazin-6-yl)oxy)methyl)-2-ethyl-

HRID 274281
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HRID 274281 반응식
CN(C=[N:5][S:6]([CH2:9][C:10]([CH2:15][CH3:16])([CH2:13][CH3:14])[CH2:11][OH:12])(=[O:8])=[O:7])C.Cl[C:18]1[CH:19]=[C:20]([CH3:28])[C:21]2[N:22]([N:24]=[C:25]([CH3:27])[N:26]=2)[N:23]=1>>[CH2:15]([C:10]([CH2:13][CH3:14])([CH2:9][S:6](=[O:7])(=[O:8])[NH2:5])[CH2:11][O:12][C:18]1[CH:19]=[C:20]([CH3:28])[C:21]2[N:22]([N:24]=[C:25]([CH3:27])[N:26]=2)[N:23]=1)[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 104876986-Chloro-2,8-dimethyl[1,2,4]triazolo[1,5-b]pyridazineHCID 536426363-(N,N-dimethylaminomethylene)aminosulfonyl-2,2-diethyl-1-propanol

생성물 1

HCID 30738001-Butanesulfonamide, 2-(((2,8-dimethyl(1,2,4)triazolo(1,5-b)pyridazin-6-yl)oxy)methyl)-2-ethyl-

실험 절차

Using 3-(N,N-dimethylaminomethylene)aminosulfonyl-2,2-diethyl-1-propanol and 6-chloro-2,8-dimethyl[1,2,4]triazolo[1,5-b]pyridazine, the same reaction as in Example 6 was conducted to produce the title compound. m.p. 159°-160° C.

후처리

  1. customthe same reaction as in Example 6

출처 및 근거

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
ORD 기록
ord-a613dde543074e8099848dab411c0346
출처 데이터셋
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05389633

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