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Potassium Carbonate → 2-methoxy-4-(1-methyl-3,6-dihydro-2H-pyridin-4-yl)-5-nitroaniline

HRID 1842671
ノート
印刷プレビュー

反応式

HRID 1842671 の反応式
Br[C:2]1[C:8]([N+:9]([O-:11])=[O:10])=[CH:7][C:5]([NH2:6])=[C:4]([O:12][CH3:13])[CH:3]=1.[CH3:14][N:15]1[CH2:20][CH:19]=[C:18](B2OC(C)(C)C(C)(C)O2)[CH2:17][CH2:16]1.C([O-])([O-])=O.[K+].[K+]>O1CCOCC1.O.CCOC(C)=O.[Pd].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>[CH3:13][O:12][C:4]1[CH:3]=[C:2]([C:18]2[CH2:19][CH2:20][N:15]([CH3:14])[CH2:16][CH:17]=2)[C:8]([N+:9]([O-:11])=[O:10])=[CH:7][C:5]=1[NH2:6]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 3

HCID 11430Potassium CarbonateHCID 207733711-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridineHCID 717431004-Bromo-2-methoxy-5-nitroaniline2 回

生成物 1

HCID 866773252-methoxy-4-(1-methyl-3,6-dihydro-2H-pyridin-4-yl)-5-nitroaniline収率 92.3%

試薬・触媒・溶媒 4

HCID 11979704
Tetrakis(triphenylphosphine)palladium
触媒
HCID 962Water溶媒
HCID 8857Ethyl Acetate溶媒
HCID 312751,4-Dioxane溶媒

実験手順

A mixture of 4-bromo-2-methoxy-5-nitroaniline (Intermediate 4, 1.112 g, 4.5 mmol), 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine (1.004 g, 4.50 mmol) and K2CO3 (2.488 g, 18.00 mmol) was stirred in 1,4-dioxane (20 mL) and water (5 mL). The mixture was purged with N2 for 0.25 h. Tetrakis(triphenylphosphine)-palladium(0) (0.052 g, 0.05 mmol) was then added and the mixture was heated at reflux for 2 h. The mixture was then cooled, filtered and the filtrate was concentrated in vacuo to give an aqueous mixture. This mixture was dissolved in EtOAc and water and the phases were separated. The aqueous solution was extracted with EtOAc. The combined organic solutions were then extracted twice with 2M HCl (40 mL). The aqueous solutions were basified with 2M Na2CO3 (50 mL) and extracted with EtOAc (3×40 mL). The combined organic solutions were dried (MgSO4) and concentrated in vacuo. The residue was dissolved in a mixture of CH2Cl2 and 2N methanolic ammonia (10:1, 10 mL) and the solution was filtered through a silica plug. The filtrate was concentrated in vacuo to give an oil which subsequently crystallised. Trituration with isohexane and diethyl ether (1:1, 5 mL) and collection of the resulting solid by filtration gave the title compound (1.093 g, 92%) as a yellow crystalline solid; 1H NMR: 2.23 (2H, dd), 2.27 (3H, s), 2.53 (2H, t), 2.93 (2H, d), 3.87 (3H, s), 5.27 (2H, s), 5.42-5.53 (1H, m), 6.65 (1H, s), 7.23 (1H, s); m/z: ES+ MH+ 264.

後処理

  1. customThe mixture was purged with N2 for 0.25 h
  2. temperaturethe mixture was heated
  3. temperatureat reflux for 2 h
  4. temperatureThe mixture was then cooled
  5. filtrationfiltered
  6. concentrationthe filtrate was concentrated in vacuo
  7. customto give an aqueous mixture
  8. customwater and the phases were separated
  9. extractionThe aqueous solution was extracted with EtOAc
  10. extractionThe combined organic solutions were then extracted twice with 2M HCl (40 mL)
  11. extractionextracted with EtOAc (3×40 mL)
  12. dry with materialThe combined organic solutions were dried (MgSO4)
  13. concentrationconcentrated in vacuo
  14. dissolutionThe residue was dissolved in a mixture of CH2Cl2 and 2N methanolic ammonia (10:1, 10 mL)
  15. filtrationthe solution was filtered through a silica plug
  16. concentrationThe filtrate was concentrated in vacuo
  17. customto give an oil which
  18. customsubsequently crystallised
  19. customTrituration with isohexane and diethyl ether (1:1, 5 mL) and collection of the resulting solid
  20. filtrationby filtration

出典と根拠

ORDレコード
ord-60e6d1916eea453f8acceef1da4d58e1
出典データセット
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08946235B2

反応ノート

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