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Triethylamine → N-(6-Methoxy-4-methyl-8-quinolinyl)-2,6-dimethyl-4-morpholinehexanamide

HRID 542854
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HRID 542854 반응식
Br[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]([NH:9][C:10]1[CH:11]=[C:12]([O:21][CH3:22])[CH:13]=[C:14]2[C:19]=1[N:18]=[CH:17][CH:16]=[C:15]2[CH3:20])=[O:8].[CH3:23][CH:24]1[O:29][CH:28]([CH3:30])[CH2:27][NH:26][CH2:25]1.C(N(CC)CC)C>C1C=CC=CC=1>[CH3:22][O:21][C:12]1[CH:13]=[C:14]2[C:19](=[C:10]([NH:9][C:7](=[O:8])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][N:26]3[CH2:25][CH:24]([CH3:23])[O:29][CH:28]([CH3:30])[CH2:27]3)[CH:11]=1)[N:18]=[CH:17][CH:16]=[C:15]2[CH3:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471Triethylamine2회HCID 1108622,6-Dimethylmorpholine2회HCID 6120236-Bromo-N-(6-methoxy-4-methyl-8-quinolinyl)hexanamide

생성물 1

HCID 13853362N-(6-Methoxy-4-methyl-8-quinolinyl)-2,6-dimethyl-4-morpholinehexanamide수율 55.1%

시약·촉매·용매 1

HCID 241Benzene용매2회

실험 절차

A mixture of 5.5 g (0.015 mole) of 6-bromo-N-(6-methoxy-4-methyl-8-quinolinyl)hexanamide and 1.85 ml (0.018 mole) of 2,6-dimethylmorpholine in 90 ml of benzene was heated under reflux for 24 hr. Triethylamine (2 ml) was added and the mixture was heated under reflux for an additional 2 hr, allowed to cool, and filtered. The filtrate was washed with water, dried and concentrated. TLC(silica gel--ethyl acetate) demonstrated a mixture of the unchanged bromo compound, Rf(silica--ethyl acetate)=0.63, and the product, Rf=0.08. A solution of the residue, 1.3 ml (0.01 mole) of 2,6-dimethylmorpholine, and 1.5 ml of triethylamine in 80 ml of benzene was heated under reflux for 40 hr, allowed to cool, filtered, washed with water, dried and concentrated. The residue was chromatographed over 200 g of silica gel with 1 liter each of the following solutions of methanol in ethyl acetate: 1.5%, 2%, 3% to afford 3.7 g of crude product. Recrystallization from hexane afforded 3.3 g of the title compound, mp 87°-90°. The NMR spectrum confirmed the presence of hexane.

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 24 hr
  3. temperaturethe mixture was heated
  4. temperatureunder reflux for an additional 2 hr
  5. temperatureto cool
  6. filtrationfiltered
  7. washThe filtrate was washed with water
  8. customdried
  9. concentrationconcentrated
  10. additiona mixture of the unchanged bromo compound, Rf(silica--ethyl acetate)=0.63
  11. temperatureunder reflux for 40 hr
  12. temperatureto cool
  13. filtrationfiltered
  14. washwashed with water
  15. customdried
  16. concentrationconcentrated
  17. customThe residue was chromatographed over 200 g of silica gel with 1 liter each of the following solutions of methanol in ethyl acetate
  18. custom1.5%, 2%, 3% to afford 3.7 g of crude product
  19. customRecrystallization from hexane

출처 및 근거

ORD 기록
ord-861a705abb484b67992aaa5135c24890
출처 데이터셋
uspto-grants-1987_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04659708

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