Tetrahydrofuran → 8-Methoxy-2-methylquinoline-5-carboxylic acid

HRID 2393086ノート

反応式

HRID 2393086 の反応式
Br[C:2]1[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[C:8]2[C:3]=1[CH:4]=[CH:5][C:6]([CH3:14])=[N:7]2.C(N(CC)CC)C.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[C]=[O:42].[O:43]1[CH2:47]CCC1>O.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.Cl[Pd]Cl>[CH3:13][O:12][C:9]1[C:8]2[N:7]=[C:6]([CH3:14])[CH:5]=[CH:4][C:3]=2[C:2]([C:47]([OH:43])=[O:42])=[CH:11][CH:10]=1

参加物

8

反応条件

温度
80 °C

実験手順

A mixtures of 5-bromo-8-methoxy-2-methylquinoline (2.0 g), triethylamine (11 ml), triphenylphosphine (0.79 g), and bis(tripbenylphosphine)palladium (II) chloride (1.56 g) in tetrahydrofuran (200 ml) and water (90 ml) was stirred in a pressurised reaction vessel and charged with carbon monoxide to a pressure of 160 psi. The vessel was heated to 80° C. and stirred for 72 hours. The reaction was allowed to cool and depressurised. The mixture was filtered ant the organic solvent was removed in vacuo. The aqueous residue was basified with 1M sodium hydroxide and washed with ethyl acetate (300ml). The aqueous solution was acidified to pH 5 with glacial acetic acid and extracted with ethyl acetate (2×400 ml). The organic extracts were combined, dried over magnesium sulphate, filtered and the filtrate evaporated in vacuo to yield the title product (1.0 g) as an off-white solid.

後処理

  1. temperatureto cool
  2. filtrationThe mixture was filtered ant the organic solvent
  3. customwas removed in vacuo
  4. washwashed with ethyl acetate (300ml)
  5. extractionextracted with ethyl acetate (2×400 ml)
  6. dry with materialdried over magnesium sulphate
  7. filtrationfiltered
  8. customthe filtrate evaporated in vacuo

出典と根拠

ORDレコード
ord-2f6f410569284a44a78b8eda99f401bd
出典データセット
uspto-grants-1998_09
特許番号
US05804588

反応ノート

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