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Methane → Gsk 894281

HRID 130465
ノート
印刷プレビュー

反応式

HRID 130465 の反応式
Br[C:2]1[CH:7]=[CH:6][C:5]([S:8]([NH:11][C:12]2[CH:17]=[C:16]([N:18]3[CH2:23][C@H:22]([CH3:24])[NH:21][C@H:20]([CH3:25])[CH2:19]3)[CH:15]=[CH:14][C:13]=2[O:26][CH3:27])(=[O:10])=[O:9])=[CH:4][C:3]=1[F:28].C(=O)([O-])[O-].[Na+].[Na+].[CH3:35][C:36]1[O:40][C:39](B(O)O)=[CH:38][CH:37]=1.C>COCCOC.O.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.C(OCC)(=O)C>[CH3:25][C@H:20]1[NH:21][C@@H:22]([CH3:24])[CH2:23][N:18]([C:16]2[CH:15]=[CH:14][C:13]([O:26][CH3:27])=[C:12]([NH:11][S:8]([C:5]3[CH:6]=[CH:7][C:2]([C:39]4[O:40][C:36]([CH3:35])=[CH:37][CH:38]=4)=[C:3]([F:28])[CH:4]=3)(=[O:10])=[O:9])[CH:17]=2)[CH2:19]1
参加物実験手順後処理出典と根拠反応ノート

参加物

9

反応物 4

HCID 297MethaneHCID 10340Sodium CarbonateHCID 27343725-Methyl-2-furanboronic Acid2 回HCID 590070604-Bromo-N-[5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)phenyl]-3-fluorobenzenesulfonamide

生成物 1

HCID 24803511Gsk 894281

試薬・触媒・溶媒 4

HCID 178418476
HCID 178418476、化合物
触媒
HCID 962Water溶媒3 回
HCID 80711,2-Dimethoxyethane溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

A stirred suspension of 4-bromo-N-[5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)phenyl]-3-fluorobenzenesulfonamide (3.4 g, 7.2 mmol) in 1,2-dimethoxyethane (80 ml) was treated with a solution of sodium carbonate (3.8 g, 36 mmol) in water (20 ml). (5-Methyl-2-furanyl)boronic acid (1.4 g, 10.8 mmol) and bis(triphenylphosphine)palladium(II) chloride (10 mg, 0.2 mol %) were added with some water and the mixture was stirred at reflux for 3 hours. Additional (5-methyl-2-furanyl)boronic acid (420 mg, 3.3 mmol) was added and the mixture was heated at reflux for a further 30 minutes. After cooling to room temperature, ethyl acetate (50 ml), water (50 ml) and charcoal (3 g) were added and the mixture was stirred at room temperature for 30 minutes. The mixture was filtered through celite, the ethyl acetate layer separated and the aqueous layer was further extracted with ethyl acetate. The ethyl acetate extracts were combined washed with water and brine dried over anhydrous sodium sulfate and evaporated. The residue was purified by chromatography on a 100 g column eluting with 1:40 to 1:10 2M ammonia in methanol: dichloromethane. Residue was then triturated in ether, dissolved in ether/pentane and evaporated. Residue was then triturated in pentane, washed in pentane, air dried and then dried at 50° C. under argon and high vacuum to give the title compound (E248). MS (ES+) m/e 474 [M+H]+.

後処理

  1. temperatureat reflux for 3 hours
  2. temperaturethe mixture was heated
  3. temperatureat reflux for a further 30 minutes
  4. stirringthe mixture was stirred at room temperature for 30 minutes
  5. filtrationThe mixture was filtered through celite
  6. customthe ethyl acetate layer separated
  7. extractionthe aqueous layer was further extracted with ethyl acetate
  8. washThe ethyl acetate extracts were combined washed with water and brine
  9. dry with materialdried over anhydrous sodium sulfate
  10. customevaporated
  11. customThe residue was purified by chromatography on a 100 g column
  12. washeluting with 1:40 to 1:10 2M ammonia in methanol
  13. customResidue was then triturated in ether
  14. dissolutiondissolved in ether/pentane
  15. customevaporated
  16. customResidue was then triturated in pentane
  17. washwashed in pentane
  18. customair dried
  19. customdried at 50° C. under argon

出典と根拠

ORDレコード
ord-c77defd276ae44979335002271b04b6c
出典データセット
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07381728B2

反応ノート

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