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Hydrochloric Acid → 2-Ethylsulfonyl-6-n-propylimidazo[1,2-b]pyridazin-3-ylsulfonamide

HRID 1160761
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HRID 1160761 반응식
[CH2:1]([S:3][C:4]1[N:5]=[C:6]2[CH:11]=[CH:10][C:9]([CH2:12][CH2:13][CH3:14])=[N:8][N:7]2[C:15]=1[S:16]([NH2:19])(=[O:18])=[O:17])[CH3:2].C([O-])([O-])=[O:21].C([O-])([O-])=O.OO.OO.OO.[Na+].[Na+].[Na+].[Na+].Cl.[OH2:39]>C(#N)C>[CH2:1]([S:3]([C:4]1[N:5]=[C:6]2[CH:11]=[CH:10][C:9]([CH2:12][CH2:13][CH3:14])=[N:8][N:7]2[C:15]=1[S:16]([NH2:19])(=[O:17])=[O:18])(=[O:21])=[O:39])[CH3:2]
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참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 962Water2회HCID 159762Sodium percarbonateHCID 230281222-Ethylthio-6-n-propylimidazo[1,2-b]pyridazin-3-ylsulfonamide

생성물 1

HCID 230281332-Ethylsulfonyl-6-n-propylimidazo[1,2-b]pyridazin-3-ylsulfonamide

시약·촉매·용매 1

HCID 6342
Acetonitrile
용매

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온도
55 °C

실험 절차

2-Ethylthio-6-n-propylimidazo[1,2-b]pyridazin-3-ylsulfonamide (0.30 g, 1.00 mmol) was suspended in acetonitrile (1.0 ml) and water (4.0 ml), and sodium percarbonate (effective oxygen concentration, 12.2%; 0.33 g; 2.50 mmol) was added thereto at 45° C. and stirred at 50 to 60° C. for 2.5 hours. The reaction mixture was poured into water and acidified with dilute hydrochloric acid, and the precipitated insoluble solids were collected by filtration and washed with water, to give the title compound as white crystals. The yield was 0.25 g (75.3%).

후처리

  1. filtrationthe precipitated insoluble solids were collected by filtration
  2. washwashed with water

출처 및 근거

ORD 기록
ord-a9aac78e05304edbab31ed6d61e29c55
출처 데이터셋
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07816526B2

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