Water → 6-Iodo-2-(methylsulfonyl)benzo[d]thiazole

HRID 1691981노트

반응식

HRID 1691981 반응식
[I:1][C:2]1[CH:12]=[CH:11][C:5]2[N:6]=[C:7]([S:9][CH3:10])[S:8][C:4]=2[CH:3]=1.[Mn]([O-])(=O)(=O)=[O:14].[K+].[OH2:19]>C(O)(=O)C>[I:1][C:2]1[CH:12]=[CH:11][C:5]2[N:6]=[C:7]([S:9]([CH3:10])(=[O:14])=[O:19])[S:8][C:4]=2[CH:3]=1

참가 물질

5

반응물 3

HCID 962WaterHCID 516875Potassium PermanganateHCID 669058856-Iodo-2-(methylthio)benzo[d]thiazole

생성물 1

HCID 669061396-Iodo-2-(methylsulfonyl)benzo[d]thiazole

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

To a stirred, room temperature solution of 6-iodo-2-(methylthio)benzo[d]thiazole (Reference Example 6b, 1.22 g, 4.0 mmol) in acetic acid (100 mL) was added dropwise a solution of potassium permanganate (0.190 g, 1.2 mmol) in water (60 mL). The reaction mixture was stirred at room temperature for 68 hours, then quenched with aqueous sodium sulfite. The resulting mixture was vigorously stirred at room temperature overnight. The resulting precipitate was collected by filtration and rinsed with water. The solid was dissolved in ethyl acetate, dried (MgSO4), and filtered. The filtrate was concentrated under reduced pressure to provide 6-iodo-2-(methylsulfonyl)benzo[d]thiazole. 1H NMR (300 MHz, CDCl3) δ ppm 3.41 (s, 3H), 7.93 (d, J=1 Hz, 2H), 8.38 (t, J=1 Hz, 1H); MS(DCI/NH3) m/z 340 (M+H)−, 357 (M+NH4)+.

후처리

  1. customquenched with aqueous sodium sulfite
  2. stirringThe resulting mixture was vigorously stirred at room temperature overnight
  3. filtrationThe resulting precipitate was collected by filtration
  4. washrinsed with water
  5. dissolutionThe solid was dissolved in ethyl acetate
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. concentrationThe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-e3d12b99d40443fcb3a317da4461c838
출처 데이터셋
uspto-grants-2012_04
특허 번호
US08153813B2

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