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Water → 2-(3-Iodophenyl)-5-methyl-1,3,4-thiadiazole

HRID 1672791
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HRID 1672791 반응식
C1(C)C=CC=CC=1.COC1C=CC(P2(SP(C3C=CC(OC)=CC=3)(=S)S2)=[S:17])=CC=1.[C:30]([NH:33][NH:34][C:35](=O)[C:36]1[CH:41]=[CH:40][CH:39]=[C:38]([I:42])[CH:37]=1)(=O)[CH3:31].O>C(OCC)(=O)C>[I:42][C:38]1[CH:37]=[C:36]([C:35]2[S:17][C:30]([CH3:31])=[N:33][N:34]=2)[CH:41]=[CH:40][CH:39]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 1140TolueneHCID 87949Lawesson's reagentHCID 824395HCID 824395, 화합물

생성물 1

HCID 193499822-(3-Iodophenyl)-5-methyl-1,3,4-thiadiazole수율 60.4%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

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온도
120 °C

실험 절차

Toluene (4.1 mL) and Lawesson's reagent (366 mg, 0.904 mmol) were added to N′-acetyl-3-iodobenzohydrazide (250 mg, 0.822 mmol) obtained in Step 1, and the mixture was stirred at 120° C. for 1 hour. After cooling, water and ethyl acetate were added to the mixture to separate the organic layer. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The resulting residue was then purified by silica gel column chromatography to give 2-(3-iodophenyl)-5-methyl-1,3,4-thiadiazole (150 mg, 60%).

후처리

  1. temperatureAfter cooling
  2. customto separate the organic layer
  3. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  4. customthe solvent was evaporated under reduced pressure
  5. customThe resulting residue was then purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-57390878c68a49b288a5e393d50076c3
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07998954B2

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