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Methanesulfonyl chloride → 2-Guanidino-4-(methanesulfonyloxymethyl)thiazole

HRID 2412459
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HRID 2412459 반응식
[NH:1]([C:5]1[S:6][CH:7]=[C:8]([CH2:10][OH:11])[N:9]=1)[C:2]([NH2:4])=[NH:3].[CH3:12][S:13](Cl)(=[O:15])=[O:14]>N1C=CC=CC=1>[NH:1]([C:5]1[S:6][CH:7]=[C:8]([CH2:10][O:11][S:13]([CH3:12])(=[O:15])=[O:14])[N:9]=1)[C:2]([NH2:4])=[NH:3]
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참가 물질

4

반응물 2

HCID 31297Methanesulfonyl chlorideHCID 178512688HCID 178512688, 화합물

생성물 1

HCID 1785052772-Guanidino-4-(methanesulfonyloxymethyl)thiazole수율 96%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

To a solution of 2-guanidino-4-hydroxymethylthiazole (0.86 g) in pyridine (6 ml) is gradually added methanesulfonyl chloride (0.6 g) under ice cooling, and the resultant mixture is stirred at room temperature for 2 hours. The reaction mixture is concentrated in vacuum, and the residual oil is chromatographed on a column of silica gel, which is eluted with methanol. The eluate is concentrated in vacuum to give 2-guanidino-4-(methanesulfonyloxymethyl)thiazole (1.2 g) as an oil. The yield is 96%.

후처리

  1. concentrationThe reaction mixture is concentrated in vacuum
  2. customthe residual oil is chromatographed on a column of silica gel, which
  3. washis eluted with methanol
  4. concentrationThe eluate is concentrated in vacuum

출처 및 근거

ORD 기록
ord-306843c60df84c56a8d782f69ef0f2b1
출처 데이터셋
uspto-grants-1985_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04492794

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