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

HRID 38820
ノート
印刷プレビュー

反応式

HRID 38820 の反応式
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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 517044Potassium Acetate2 回HCID 2733548Bis(pinacolato)diborane2 回HCID 59519513N-(5-bromo-2-chloro-3-pyridinyl)methanesulfonamide

生成物 1

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

試薬・触媒・溶媒 2

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

反応条件

温度
90 °C

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-82e7ad5be2de4aa788c29886c0801d9c
出典データセット
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08524751B2

反応ノート

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