Methyl iodide → 2-(5,7-Difluoro-quinolin-6-yl)-propionic acid methyl ester

HRID 456112노트

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HRID 456112 반응식
[Li+].[CH3:2]C([N-]C(C)C)C.[CH3:9][O:10][C:11](=[O:25])[CH2:12][C:13]1[C:14]([F:24])=[C:15]2[C:20](=[CH:21][C:22]=1[F:23])[N:19]=[CH:18][CH:17]=[CH:16]2.CI>C1COCC1>[CH3:9][O:10][C:11](=[O:25])[CH:12]([C:13]1[C:14]([F:24])=[C:15]2[C:20](=[CH:21][C:22]=1[F:23])[N:19]=[CH:18][CH:17]=[CH:16]2)[CH3:2]

참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 2724682Lithium diisopropylamideHCID 58190558Methyl 2-(5,7-difluoroquinolin-6-yl)acetate

생성물 1

HCID 581905742-(5,7-Difluoro-quinolin-6-yl)-propionic acid methyl ester수율 95.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To a solution of LDA (1.2 M in THF, 9.5 mL, 11.40 mmol) in dry THF (30 mL) at −78° C. was added dropwise a solution of (5,7-difluoroquinolin-6-yl)-acetic acid methyl ester (2.12 g, 9.50 mmol) in THF (20 mL). After 30 min, MeI (0.9 mL, 14.25 mmol) was added dropwise, and the reaction mixture was allowed to rise to 0° C. slowly. After 1 h, the reaction was quenched by satd. aq. NaHCO3 solution, and extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous Na2SO4, filtered, concentrated, and purified by flash chromatography to afford 2.272 g of the title compound as pale yellow solid. 1H-NMR (400 MHz, CDCl3) δ ppm 8.93 (d, 1H), 8.39 (dd, 1H), 7.61 (dd, 1H), 7.41-7.46 (m, 1H), 4.29 (q, 1H), 3.73 (s, 3H), 1.62 (d, 3H). LCMS (method A): [MH]+=252, tR=5.09 min.

후처리

  1. customto rise to 0° C.
  2. waitAfter 1 h
  3. customthe reaction was quenched by satd
  4. extractionaq. NaHCO3 solution, and extracted with EtOAc
  5. washThe organic layer was washed with brine
  6. dry with materialdried over anhydrous Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated
  9. custompurified by flash chromatography

출처 및 근거

ORD 기록
ord-450b46fec419408aa8989414c7a77bb9
출처 데이터셋
uspto-grants-2013_07
특허 번호
US08497368B2

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