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Methyl iodide → HCID 71279836、化合物

HRID 246056
ノート
印刷プレビュー

反応式

HRID 246056 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6328Methyl iodideHCID 23665647Potassium tert-butoxideHCID 178506571HCID 178506571、化合物

生成物 1

HCID 71279836HCID 71279836、化合物収率 55.3%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
0 °C

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-5ef64902ce0b4bcbbd411dc3d5c027fe
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08658646B2

反応ノート

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