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Imidazole → Pyrimidine, 2-(1,1-difluoro-2-iodoethyl)-

HRID 1171070
ノート
印刷プレビュー

反応式

HRID 1171070 の反応式
[F:1][C:2]([F:11])([C:5]1[N:10]=[CH:9][CH:8]=[CH:7][N:6]=1)[CH2:3]O.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.N1C=CN=C1.[I:36]I>C1(C)C=CC=CC=1.CC#N>[F:1][C:2]([C:5]1[N:10]=[CH:9][CH:8]=[CH:7][N:6]=1)([F:11])[CH2:3][I:36]
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

7

反応物 4

HCID 795ImidazoleHCID 807IodineHCID 11776TriphenylphosphineHCID 589729572-Pyrimidineethanol, beta,beta-difluoro-

生成物 1

HCID 58973005Pyrimidine, 2-(1,1-difluoro-2-iodoethyl)-収率 73%

試薬・触媒・溶媒 2

HCID 1140Toluene溶媒
HCID 6342
Acetonitrile
溶媒

反応条件

温度
0 °C

実験手順

A homogeneous solution of 2,2-difluoro-2-pyrimidin-2-yl-ethanol (689 mg, 4.31 mmol), as prepared in the previous step, PPh3 (1.69 g, 6.44 mmol), and imidazole (590 mg, 8.67 mmol) in toluene (5.8 mL) and CH3CN (2.9 mL) was stirred at 0° C. for 5 min, and was then treated with I2 (1.61 g, 6.34 mmol) in two portions and stirred at 0° C. for another 5 min. The resulting brown opaque slurry was then heated at 90° C. for 19 h, and then allowed to cool to rt. The mixture was filtered, the beige filter cake was washed with toluene (3×10 mL), and the combined brown filtrates were concentrated. Silica flash chromatography of the residue (2:1 hex/EtOAc eluent) afforded the title compound as a pale yellow oil (849 mg, 73%).

後処理

  1. stirringstirred at 0° C. for another 5 min
  2. temperatureThe resulting brown opaque slurry was then heated at 90° C. for 19 h
  3. temperatureto cool to rt
  4. filtrationThe mixture was filtered
  5. washthe beige filter cake was washed with toluene (3×10 mL)
  6. concentrationthe combined brown filtrates were concentrated

出典と根拠

ORDレコード
ord-2a5d9b66031e426f860c36afcf83578d
出典データセット
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07829584B2

反応ノート

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