반응 #1929078

ord-a73ab42e0f114071ba1c5c3b5bcae1e4

반응 방정식

Cl
hydrogen chloride
OB(O)c1ccc(Cl)c(F)c1
(4-chloro-3-fluorophenyl)boronic acid
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
Cc1ccc(Br)cc1C1=C(O)C2(CCCCC2)NC1=O
compound
Cc1ccc(Br)cc1C1=C(O)C2(CCCCC2)NC1=O
3-(5-Bromo-2-methylphenyl)-4-hydroxy-1-azaspiro[4.5]dec-3-en-2-one
O=S(=O)([O-])[O-].[Mg+2]
magnesium sulfate
Cc1ccc(-c2ccc(Cl)c(F)c2)cc1C1=C(O)C2(CCCCC2)NC1=O
title compound
Cc1ccc(-c2ccc(Cl)c(F)c2)cc1C1=C(O)C2(CCCCC2)NC1=O
3-(4′-Chloro-3′-fluoro-4-methylbiphenyl-3-yl)-4-hydroxy-1-azaspiro[4.5]dec-3-en-2-one

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타Under microwave irradiation
  2. 2
    온도the reaction mixture was heated at 150° C. for 10 minutes
  3. 3
    온도After cooling
  4. 4
    여과the mixture was filtered through silica gel
  5. 5
    세척the filter cake was washed with ethyl acetate
  6. 6
    농축the mixture was concentrated
  7. 7
    기타Purification of the crude product by HPLC chromatography (C18 phase, mobile phase

실험 절차

Under argon, 36.4 mg (0.05 mmol) of dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium complex were added to 150 mg (0.45 mmol) of the compound from Example 13A in 15 ml of degassed 1,2-dimethoxyethane. The mixture was stirred at room temperature for 5 minutes, and 117 mg (0.67 mmol) of (4-chloro-3-fluorophenyl)boronic acid and a solution of 509 mg (1.56 mmol) of cesium carbonate in 0.9 ml of degassed water was then added. Under microwave irradiation, the reaction mixture was heated at 150° C. for 10 minutes. After cooling, 0.3 ml of concentrated aqueous hydrogen chloride solution were added, magnesium sulfate was added, the mixture was filtered through silica gel, the filter cake was washed with ethyl acetate and the mixture was concentrated. Purification of the crude product by HPLC chromatography (C18 phase, mobile phase: water/acetonitrile gradient/0.1% formic acid) gave 43.7 mg (25% of theory) of the title compound.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08946124B2uspto-grants-2015_02