Trifluoroacetic acid → 4-{1-[(2E)-but-2-en-1-yloxy]ethyl}-6-(2-methoxyphenyl)-2,2-dimethyl-1,2-dihydroquinoline

HRID 25784

反応式

HRID 25784 の反応式
C(OC([N:8]1[C:17]2[C:12](=[CH:13][C:14]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=3[O:24][CH3:25])=[CH:15][CH:16]=2)[C:11]([CH:26]([O:28][CH2:29]/[CH:30]=[CH:31]/[CH3:32])[CH3:27])=[CH:10][C:9]1([CH3:34])[CH3:33])=O)(C)(C)C.FC(F)(F)C(O)=O>C(Cl)Cl>[CH2:29]([O:28][CH:26]([C:11]1[C:12]2[C:17](=[CH:16][CH:15]=[C:14]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=3[O:24][CH3:25])[CH:13]=2)[NH:8][C:9]([CH3:34])([CH3:33])[CH:10]=1)[CH3:27])/[CH:30]=[CH:31]/[CH3:32]

参加物

4

実験手順

A mixture of 58 mg of [4-{1-[((E)-but-2-enyl)oxy]ethyl}-6-(2-methoxyphenyl)-2,2-dimethyl-2H-quinoline-1-carboxylic acid tert-butyl ester in 2 mL of methylene chloride was treated with 0.05 mL of 99% trifluoroacetic acid (TFA) at room temperature. The reaction mixture was allowed to stir at the same temperature for 1 hour. TLC showed starting material was still remaining so another 0.05 mL of TFA was added. Ten minutes later, the reaction was quenched with water and extracted with EtOAc three times. The organic layers were combined, washed sequentially with water, saturated aqueous sodium bicarbonate, water, brine, dried with magnesium sulfate, and the solvent evaporated in vacuo. The residue was purified by flash chromatography to yield 28 mg of the title compound as an oil.

後処理

  1. additionwas added
  2. customTen minutes later, the reaction was quenched with water
  3. extractionextracted with EtOAc three times
  4. washwashed sequentially with water, saturated aqueous sodium bicarbonate, water, brine
  5. dry with materialdried with magnesium sulfate
  6. customthe solvent evaporated in vacuo
  7. customThe residue was purified by flash chromatography

出典と根拠

ORDレコード
ord-1ea488f2001a4e0ea6289d4fd9ea2e95
出典データセット
uspto-grants-2005_02
特許番号
US06858627B2

関連ノート

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