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Ethyl chloroformate → HCID 69130224、化合物

HRID 2253268
ノート
印刷プレビュー

反応式

HRID 2253268 の反応式
[CH3:1][O:2][C:3](=[O:34])[C:4]([C:16]1[CH:21]=[CH:20][C:19]([O:22][C:23]2[CH:28]=[CH:27][C:26]([CH2:29][CH2:30][C:31](=[O:33])[NH2:32])=[CH:25][CH:24]=2)=[CH:18][CH:17]=1)=[CH:5][C:6]1[CH:11]=[C:10]([O:12][CH3:13])[CH:9]=[C:8]([O:14][CH3:15])[CH:7]=1.C([N-]C(C)C)(C)C.[Li+].Cl[C:44]([O:46][CH2:47][CH3:48])=[O:45]>C1COCC1>[CH3:1][O:2][C:3](=[O:34])[C:4]([C:16]1[CH:21]=[CH:20][C:19]([O:22][C:23]2[CH:24]=[CH:25][C:26]([CH2:29][CH2:30][C:31]([NH:32][C:44]([O:46][CH2:47][CH3:48])=[O:45])=[O:33])=[CH:27][CH:28]=2)=[CH:18][CH:17]=1)=[CH:5][C:6]1[CH:11]=[C:10]([O:12][CH3:13])[CH:9]=[C:8]([O:14][CH3:15])[CH:7]=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 10928Ethyl chloroformateHCID 2724682Lithium diisopropylamideHCID 69130631HCID 69130631、化合物

生成物 1

HCID 69130224HCID 69130224、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-78 °C

実験手順

2-{4-[4-(2-Carbamoyl-ethyl)-phenoxy]-phenyl }-3-(3,5-dimethoxyphenyl)-acrylic acid methyl ester (7) was obtained as a byproduct in the synthesis of 3-(3,5-dimethoxy-phenyl)-2-{4-[4-(2,4-dioxothiazolidin-5-ylmethyl)-phenoxy]-phenyl}-acrylic acid methyl ester, performed essentially as shown in PCT/US99/09982 (WO 99/58127). 7 (460 mg, 1.0 mmol) was taken up in dry THF (6 mL) and cooled to −78° C. To this solution, lithium diisopropyl amide (LDA) (2M, 0.55 mL, 1.1 mmol) was added and stirred for 10 min. Ethyl chloroformate (0.11 mL, 1.2 mmol) was added and stirred overnight at room temperature. The reaction was quenched with saturated aqueous ammonium chloride solution and ethyl acetate (50 mL) was added. The organic layer was washed with brine (2×20 mL), dried on anhydrous magnesium sulfate and evaporated under reduced pressure. The crude product was purified by silica gel chromatography and eluted with hexane-ethyl acetate (7:3). Yield: 264 mg, 49.8%.

後処理

  1. stirringstirred overnight at room temperature
  2. customThe reaction was quenched with saturated aqueous ammonium chloride solution and ethyl acetate (50 mL)
  3. additionwas added
  4. washThe organic layer was washed with brine (2×20 mL)
  5. dry with materialdried on anhydrous magnesium sulfate
  6. customevaporated under reduced pressure
  7. customThe crude product was purified by silica gel chromatography
  8. washeluted with hexane-ethyl acetate (7:3)

出典と根拠

ORDレコード
ord-830ef66c1dd540d495bb59c68f6fccd8
出典データセット
uspto-grants-2008_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07323496B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート