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Methyl iodide → HCID 71279836, 화합물

HRID 246056
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HRID 246056 반응식
[I:1][C:2]1[C:3]2[S:9][CH:8]=[CH:7][C:4]=2[NH:5][N:6]=1.[CH3:10]C([O-])(C)C.[K+].IC>C1COCC1>[I:1][C:2]1[C:3]2[S:9][CH:8]=[CH:7][C:4]=2[N:5]([CH3:10])[N:6]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 23665647Potassium tert-butoxideHCID 178506571HCID 178506571, 화합물

생성물 1

HCID 71279836HCID 71279836, 화합물수율 55.3%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

To a solution of 3-iodo-1H-thieno[3,2-c]pyrazole (500 mg, 2.0 mmol) in THF (7 ml) at 0° C. was added KOt-Bu (314 mg, 2.8 mmol). The reaction mixture was stirred at 0° C. for 30 min then added iodomethane (0.17 ml, 2.8 mmol). Stirred at 0° C. for 30 min then warmed to room temperature and stirred for 1.5 h. The reaction was quenched with water and extracted with EtOAc (2×). The combined organics were washed with brine then dried over MgSO4 and concentrated. The crude residue was purified by silica gel chromatography with 20% to 50% EtOAc/heptane to afford 292 mg (55%) of 3-iodo-1-methyl-1H-thieno[3,2-c]pyrazole as a light brown viscous oil. 1H NMR (CDCl3, 300 MHz): δ (ppm) 7.41 (d, J=5.3 Hz, 1H), 6.97 (d, J=5.3 Hz, 1H), 4.05 (s, 3H). Also isolated 141 mg (27%) of 3-iodo-2-methyl-2H-thieno[3,2-c]pyrazole as an off-white solid. 1H NMR (CDCl3, 300 MHz): δ (ppm) 7.36 (d, J=5.3 Hz, 1H), 7.16 (d, J=5.3 Hz, 1H), 4.13 (s, 3H).

후처리

  1. stirringStirred at 0° C. for 30 min
  2. temperaturethen warmed to room temperature
  3. stirringstirred for 1.5 h
  4. customThe reaction was quenched with water
  5. extractionextracted with EtOAc (2×)
  6. washThe combined organics were washed with brine
  7. dry with materialthen dried over MgSO4
  8. concentrationconcentrated
  9. customThe crude residue was purified by silica gel chromatography with 20% to 50% EtOAc/heptane

출처 및 근거

ORD 기록
ord-5ef64902ce0b4bcbbd411dc3d5c027fe
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08658646B2

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