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Isopropyl iodide → HCID 67261906, 화합물

HRID 2359095
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HRID 2359095 반응식
[Cl:1][C:2]1[S:6][C:5]([C:7]2[C:11]([I:12])=[C:10]([CH3:13])[NH:9][N:8]=2)=[CH:4][CH:3]=1.[H-].[Na+].I[CH:17]([CH3:19])[CH3:18].[Cl-].[NH4+]>CN(C)C=O>[Cl:1][C:2]1[S:6][C:5]([C:7]2[C:11]([I:12])=[C:10]([CH3:13])[N:9]([CH:17]([CH3:19])[CH3:18])[N:8]=2)=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6362Isopropyl iodideHCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 67260755HCID 67260755, 화합물

생성물 1

HCID 67261906HCID 67261906, 화합물수율 67%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
0 °C

실험 절차

3-(5-Chloro-2-thienyl)-4-iodo-5-methyl-1H-pyrazole (31.9 mmol) was dissolved in 30 mL dry N,N-dimethylformamide and cooled to 0° C. under nitrogen atmosphere. Sodium hydride (33.5 mmol, 60% dispersion in mineral oil) was added in portions at 0° C. After stirring for 30 min, 2-iodopropane (38.5 mmol) was added dropwise. The reaction mixture was allowed to warm to room temperature and was stirred overnight. The solution was poured into saturated aqueous ammonium chloride solution and extracted with diethyl ether, dried over MgSO4, filtered and evaporated. The crude product was purified by chromatography on silica gel (cyclohexane:dichloromethane 90:10) to afford 7.5 g 3-(5-chloro-2-thienyl)-4-iodo-1-isopropyl-5-methyl-1H-pyrazole (67% yield)

후처리

  1. temperatureto warm to room temperature
  2. stirringwas stirred overnight
  3. extractionextracted with diethyl ether
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. customevaporated
  7. customThe crude product was purified by chromatography on silica gel (cyclohexane:dichloromethane 90:10)

출처 및 근거

ORD 기록
ord-b55883684b81446fad7505b2520803cf
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08685974B2

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