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Dimethylsulphamoyl chloride → 3-(N,N-dimethylamino)sulfonylaminomethylimidazo[5,1-b]thiazole

HRID 1603472
ノート
印刷プレビュー

反応式

HRID 1603472 の反応式
[NH2:1][CH2:2][C:3]1[N:4]2[CH:10]=[N:9][CH:8]=[C:5]2[S:6][CH:7]=1.[CH3:11][N:12]([CH3:17])[S:13](Cl)(=[O:15])=[O:14].C(=O)([O-])O.[Na+]>ClCCl.CN(C)C1C=CN=CC=1>[CH3:11][N:12]([S:13]([NH:1][CH2:2][C:3]1[N:4]2[CH:10]=[N:9][CH:8]=[C:5]2[S:6][CH:7]=1)(=[O:15])=[O:14])[CH3:17]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 83372Dimethylsulphamoyl chlorideHCID 516892Sodium BicarbonateHCID 196051553-Aminomethylimidazo[5,1-b]thiazole

生成物 1

HCID 196051593-(N,N-dimethylamino)sulfonylaminomethylimidazo[5,1-b]thiazole

試薬・触媒・溶媒 2

HCID 142844-(Dimethylamino)pyridine触媒HCID 6344Dichloromethane
溶媒

実験手順

A 210 mg potion of 3-aminomethylimidazo[5,1-b]thiazole was dissolved in 4 ml of dichloromethane, and 202 mg of 4-dimethylaminopyridine and 0.179 ml of N,N-dimethylsulfamoyl chloride were further added, followed by stirring for 2.5 hours. Then, to the reaction solution, an aqueous semi-saturated sodium hydrogencarbonate solution were added, and extraction was then carried out three times with dichloromethane. The organic layer was dried over anhydrous magnesium sulfate and then filtered, and the solvent was then evaporated under reduced pressure. Afterward, the resulting residue was purified by a silica gel column chromatograph to obtain 177 mg of the title compound.

後処理

  1. extractionextraction
  2. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  3. filtrationfiltered
  4. customthe solvent was then evaporated under reduced pressure
  5. customAfterward, the resulting residue was purified by a silica gel column chromatograph

出典と根拠

ORDレコード
ord-2bf87ac148364d89b828ac028027a872
出典データセット
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05990101

反応ノート

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