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

HRID 1603472
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HRID 1603472 반응식
[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]
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참가 물질

6

반응물 3

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

생성물 1

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

시약·촉매·용매 2

HCID 142844-(Dimethylamino)pyridine촉매HCID 6344
Dichloromethane
용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-2bf87ac148364d89b828ac028027a872
출처 데이터셋
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05990101

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