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Potassium Carbonate → 3-Chloro-6-vinylpyridazine

HRID 655257
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HRID 655257 반응식
[Cl:1][C:2]1[N:3]=[N:4][C:5](Cl)=[CH:6][CH:7]=1.[CH:9](B(O)O)=[CH2:10].C(=O)([O-])[O-].[K+].[K+].O1CCOCC1>C1C=CC([PH+]([C]2[CH][CH][CH][CH]2)C2C=CC=CC=2)=CC=1.C1C=CC([PH+]([C]2[CH][CH][CH][CH]2)C2C=CC=CC=2)=CC=1.C(Cl)Cl.Cl[Pd]Cl.[Fe].O>[Cl:1][C:2]1[N:3]=[N:4][C:5]([CH:9]=[CH2:10])=[CH:6][CH:7]=1
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참가 물질

7

반응물 4

HCID 11430Potassium CarbonateHCID 312751,4-DioxaneHCID 673313,6-DichloropyridazineHCID 4683185Vinylboronic acid

생성물 1

HCID 223362693-Chloro-6-vinylpyridazine수율 92%

시약·촉매·용매 2

HCID 53485975CID 53485975
촉매
HCID 962Water용매

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온도
80 °C

실험 절차

A mixture of 3,6-dichloropyridazine (6 g, 40.3 mmol), vinyl boronic acid pinnacol ester (6.21 g, 6.83 mL, 40.3 mmol), potassium carbonate (120 mmol, 16.7 g), 1,4-dioxane (60 mL) and water (24 mL) was degassed for 15 min with nitrogen gas. Dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct (0.4 mmol, 292 mg) was then added and the mixture heated to 80° C. for 4 hours. The aqueous phase was then removed via pipette and the organic phase concentrated onto silica gel and purified via flash column chromatography (SiO2, hexane:ethyl acetate 100:0-60:40) to return the title compound as a white solid (5.2 g, 92% yield). 1H NMR (CDCl3): δ 5.75 (1H, d), 6.25 (1H, d), 7.05 (1H, dd), 7.49 (1H, d), 7.59 (1H, d). MS m/z=141 (M+H+)+.

후처리

  1. customwas degassed for 15 min with nitrogen gas
  2. customThe aqueous phase was then removed via pipette
  3. concentrationthe organic phase concentrated onto silica gel
  4. custompurified via flash column chromatography (SiO2, hexane:ethyl acetate 100:0-60:40)

출처 및 근거

ORD 기록
ord-c960ad76935c4fe3a9da369c2fad3307
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08071581B2

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