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Hydrogen Peroxide → 5-Amino-2-(tert-butylsulfinyl)-4-phenylthiazole

HRID 1296186
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HRID 1296186 반응식
[NH2:1][C:2]1[S:6][C:5]([S:7][C:8]([CH3:11])([CH3:10])[CH3:9])=[N:4][C:3]=1[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.[OH:18]O>C(O)(=O)C>[NH2:1][C:2]1[S:6][C:5]([S:7]([C:8]([CH3:11])([CH3:9])[CH3:10])=[O:18])=[N:4][C:3]=1[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1
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참가 물질

4

반응물 2

HCID 784Hydrogen PeroxideHCID 58911918HCID 58911918, 화합물

생성물 1

HCID 667209965-Amino-2-(tert-butylsulfinyl)-4-phenylthiazole

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

To 5-amino-2-(tert-butylsulfanyl)-4-phenylthiazole (102 mg, 385 μmol) in acetic acid (5.0 ml) was added aqueous hydrogen peroxide (218 μl, 30% wt, 1.9 mmol) dropwise at ambient temperature. After 5 hr the mixture was partitioned between dichloromethane (50 ml) and water (50 ml). The aqueous phase was separated and extracted with dichloromethane (20 ml). The combined organic phases were washed with saturated aqueous sodium bicarbonate, dried over sodium sulfate, filtered and concentrated in vacuo to yield essentially pure 5-amino-2-(tert-butylsulfinyl)-4-phenylthiazole (110 mg, quant.).

후처리

  1. customdropwise at ambient temperature
  2. customAfter 5 hr the mixture was partitioned between dichloromethane (50 ml) and water (50 ml)
  3. customThe aqueous phase was separated
  4. extractionextracted with dichloromethane (20 ml)
  5. washThe combined organic phases were washed with saturated aqueous sodium bicarbonate
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-7cd250d104ae418e9d1064945c73bcc7
출처 데이터셋
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07244851B2

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