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

HRID 2393086노트

반응식

HRID 2393086 반응식
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

참가 물질

8

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온도
80 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-2f6f410569284a44a78b8eda99f401bd
출처 데이터셋
uspto-grants-1998_09
특허 번호
US05804588

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