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Potassium Acetate → {6-Chloro-5-[(methylsulfonyl)amino]-3-pyridinyl}boronic acid

HRID 38820
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HRID 38820 반응식
Br[C:2]1[CH:3]=[C:4]([NH:9][S:10]([CH3:13])(=[O:12])=[O:11])[C:5]([Cl:8])=[N:6][CH:7]=1.C([O-])(=O)C.[K+].CC1(C)C(C)(C)[O:23][B:22](B2OC(C)(C)C(C)(C)O2)[O:21]1>O1CCOCC1.[Pd](Cl)Cl.C1(P(C2C=CC=CC=2)[C-]2C=CC=C2)C=CC=CC=1.[C-]1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=C1.[Fe+2]>[Cl:8][C:5]1[N:6]=[CH:7][C:2]([B:22]([OH:23])[OH:21])=[CH:3][C:4]=1[NH:9][S:10]([CH3:13])(=[O:12])=[O:11]
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참가 물질

6

반응물 3

HCID 517044Potassium Acetate2회HCID 2733548Bis(pinacolato)diborane2회HCID 59519513N-(5-bromo-2-chloro-3-pyridinyl)methanesulfonamide

생성물 1

HCID 86653303{6-Chloro-5-[(methylsulfonyl)amino]-3-pyridinyl}boronic acid수율 111.7%

시약·촉매·용매 2

HCID 44119782
Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)
촉매
HCID 312751,4-Dioxane용매

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온도
90 °C

실험 절차

N-(5-Bromo-2-chloro-3-pyridinyl)methanesulfonamide (5 g, 17.51 mmol), potassium acetate (5.16 g, 52.5 mmol), 4,4,4′,4′,5,5,5′,5′-octamethyl-2,2′-bi-1,3,2-dioxaborolane (4.89 g, 19.26 mmol) and 1,1′-bis(diphenylphosphino)ferrocene palladium dichloride (1.281 g, 1.751 mmol) were placed in 1,4-dioxane (51 ml) and the mixture heated for 16 h at 90° C. The reaction was left stirring at 90° C. for a further 5 h. Further catalyst (0.3 g), potassium acetate (1.7 g) and 4,4,4′,4′,5,5,5′,5′-octamethyl-2,2′-bi-1,3,2-dioxaborolane (1.5 g) were added and the mixture stirred at 95° C. overnight. The mixture was cooled to room temperature then the mixture was filtered through a hydrophobic frit and the solvent removed in vacuo. The residue was partitioned between water (250 ml) and dichloromethane (250 ml). the organic layer was collected and the solvent removed in vacuo. The residue was columned on silica (3×100 g) cartridges eluting with 0-25% methanol in dichloromethane over 40 mins gave the title compound as a dark brown oil (4.9 g).

후처리

  1. waitThe reaction was left
  2. stirringthe mixture stirred at 95° C. overnight
  3. temperatureThe mixture was cooled to room temperature
  4. filtrationthe mixture was filtered through a hydrophobic frit
  5. customthe solvent removed in vacuo
  6. customThe residue was partitioned between water (250 ml) and dichloromethane (250 ml)
  7. customthe organic layer was collected
  8. customthe solvent removed in vacuo
  9. washeluting with 0-25% methanol in dichloromethane over 40 mins

출처 및 근거

ORD 기록
ord-82e7ad5be2de4aa788c29886c0801d9c
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08524751B2

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