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6-Bromoquinoxaline → 1-(Quinoxalin-6-yl)ethanone

HRID 1271385
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HRID 1271385 반응식
Br[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][CH:6]=[N:5]2.[CH2:12]([O:14]C([Sn](CCCC)(CCCC)CCCC)=C)[CH3:13].F[B-](F)(F)F.C([PH+](C(C)(C)C)C(C)(C)C)(C)(C)C>CN(C=O)C.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[N:8]1[C:9]2[C:4](=[CH:3][C:2]([C:12](=[O:14])[CH3:13])=[CH:11][CH:10]=2)[N:5]=[CH:6][CH:7]=1
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참가 물질

6

반응물 3

HCID 6109396-BromoquinoxalineHCID 619414Stannane, tributyl(1-ethoxyethenyl)-HCID 2734635Tri-tert-butylphosphine tetrafluoroborate

생성물 1

HCID 226312491-(Quinoxalin-6-yl)ethanone수율 51.1%

시약·촉매·용매 2

HCID 167845palladium(II) acetate촉매
HCID 6228
Dimethylformamide
용매

실험 절차

A solution of 6-bromo-quinoxaline (261 mg, 1.25 mmol), 1-ethoxyvinyltri-n-butyltin (0.47 mL, 1.4 mmol), palladium(II) acetate (16 mg) and tri-t-butylphosphonium tetrafluoroborate (41 mg) in anhydrous DMF (4 mL) under a nitrogen atmosphere was heated at 120° C. for 1 hr. The reaction mixture was cooled to ambient temperature and partitioned between ethyl acetate (25 mL) and H2O (10 mL). The organic extraction was washed with brine, dried (MgSO4), filtered, and concentrated. The concentrate was chromatographed on silica gel eluting with ethyl acetate:hexanes (1:1) to provide 110 mg of the title compound. 1H NMR (300 MHz, CDCl3) δ 2.79 (s, 3 H), 8.18 (d, J=9 Hz, 1 H), 8.36 (dd, J=9 Hz, J=3 Hz, 1 H), 8.70 (d, J=3 Hz, 1 H), 8.95 (s, 2 H); MS (DCl/NH3) m/z 173 (M+H)+.

후처리

  1. custompartitioned between ethyl acetate (25 mL) and H2O (10 mL)
  2. extractionThe organic extraction
  3. washwas washed with brine
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe concentrate was chromatographed on silica gel eluting with ethyl acetate:hexanes (1:1)

출처 및 근거

ORD 기록
ord-bf69d84871384c1eb6111f8fa0db674c
출처 데이터셋
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07205316B2

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