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Dimethylformamide → 2-Amino-5-(3-pyridylsulfonyl)thiazole

HRID 1656999
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HRID 1656999 반응식
[NH2:1][C:2]1[S:3][C:4]([S:7]([C:9]2[CH:10]=[N:11][CH:12]=[CH:13][CH:14]=2)=[O:8])=[CH:5][N:6]=1.ClC1C=CC=C(C(OO)=[O:23])C=1.ClCCl.CN(C)C=O>C(Cl)(Cl)Cl>[NH2:1][C:2]1[S:3][C:4]([S:7]([C:9]2[CH:10]=[N:11][CH:12]=[CH:13][CH:14]=2)(=[O:23])=[O:8])=[CH:5][N:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6228DimethylformamideHCID 6344DichloromethaneHCID 70297m-Chloroperbenzoic acidHCID 157291972-Amino-5-(3-pyridylsulfinyl)thiazole

생성물 1

HCID 157291982-Amino-5-(3-pyridylsulfonyl)thiazole수율 17.5%

시약·촉매·용매 1

HCID 6212Chloroform
용매

실험 절차

A mixture of 2-amino-5-(3-pyridylsulfinyl)thiazole (1.6 g) and 3-chloroperbenzoic acid (1.8 g) in a mixture of chloroform (150 ml), dichloromethane (50 ml) and N,N-dimethylformamide (5 ml) was stirred at room temperature for 3 hours. The reaction mixture was extracted with diluted hydrochloric acid and washed with ethyl acetate. The aqueous layer was adjusted to pH 8.5 using sodium bicarbonate and the mixture was extracted with a mixture of tetrahydrofuran and ethyl acetate (1:1). The organic layer was washed with water and dried over magnesium sulfate. The solvent was concentrated under reduced pressure and the residue was triturated with ethanol to give 2-amino-5-(3-pyridylsulfonyl)thiazole (0.30 g, yield: 17.5%). mp: 218°-220° C. (dec.) IR (Nujol): 3420, 3300, 1650, 1520, 1310 cm-1

후처리

  1. extractionThe reaction mixture was extracted with diluted hydrochloric acid
  2. washwashed with ethyl acetate
  3. extractionthe mixture was extracted with a mixture of tetrahydrofuran and ethyl acetate (1:1)
  4. washThe organic layer was washed with water
  5. dry with materialdried over magnesium sulfate
  6. concentrationThe solvent was concentrated under reduced pressure
  7. customthe residue was triturated with ethanol

출처 및 근거

ORD 기록
ord-418566edce9c48d4b4ae1a46e8edb203
출처 데이터셋
uspto-grants-1993_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05256675

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