Potassium Carbonate → 4,5-diiodo-2-cyclopropyl-1-methyl-1H-imidazole

HRID 2267181

反応式

HRID 2267181 の反応式
[I:1][C:2]1[N:3]=[C:4]([CH:8]2[CH2:10][CH2:9]2)[N:5]([CH3:7])[CH:6]=1.Cl.BrC1N=C(C2CC2)N(C)C=1.C1(C2N(C)C=CN=2)CC1.C([O-])([O-])=O.[K+].[K+].C1C(=O)N([I:44])C(=O)C1>C(OC(C)C)(=O)C>[I:1][C:2]1[N:3]=[C:4]([CH:8]2[CH2:10][CH2:9]2)[N:5]([CH3:7])[C:6]=1[I:44]

参加物

7

反応条件

温度
75 °C

実験手順

4-Iodo-2-cyclopropyl-1-methyl-1H-imidazole, 5k′. To a solution of 2-cyclopropyl-1-methyl-1H-imidazole (4a) (5.5 g, 45.0 mmol) in isopropyl acetate (110 mL) was added K2CO3 (1.25 g, 9.0 mmol) followed by NIS (40.3 g, 179.1 mmol) in portions over 2 h. The solution was stirred at 75° C. for 3 h, allowed to cool to room temperature and quenched with a 10% aqueous solution of K2CO3. The organic layer was washed with 10% K2CO3. The combined organic layers were concentrated affording crude 4,5-diiodo-2-cyclopropyl-1-methyl-1H-imidazole (10.5 g) as a dark solid. A solution of the resulting solid in THF (100 mL) was cooled to −20° C. and treated with 2 M i-PrMgCl in THF (17.5 mL, 35.0 mmol) dropwise. The reaction mixture was quenched with water and filtered. The organic layer was washed with brine and water, and concentrated afford 5k′ (8.64 g, 77% yield) as a dark orange oil. 1H-NMR (400 MHz, CDCl3) δ 6.85 (s, 1H), 3.66 (s, 3H), 1.74 (dt, J=8.4, 5.2 Hz, 1H), 1.03-0.91 (m, 4H); 13C-NMR (100 MHz, CDCl3) δ 151.9, 125.8, 79.1, 32.5, 6.9, 6.8.

後処理

  1. temperatureto cool to room temperature
  2. customquenched with a 10% aqueous solution of K2CO3
  3. washThe organic layer was washed with 10% K2CO3
  4. concentrationThe combined organic layers were concentrated

出典と根拠

ORDレコード
ord-f3c334e7089048ccbd0929c148623828
出典データセット
uspto-grants-2010_12
特許番号
US07858804B2

関連ノート

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