4-Methylmorpholine → 2'-Chloro-5'-(2-fluoro-4-morpholin-4-yl-phenylcarbamoyl)-biphenyl-4-carboxylic acid ethyl ester

HRID 1678534Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1678534
[CH2:1]([O:3][C:4]([C:6]1[CH:11]=[CH:10][C:9]([C:12]2[C:17]([Cl:18])=[CH:16][CH:15]=[C:14]([C:19]([OH:21])=O)[CH:13]=2)=[CH:8][CH:7]=1)=[O:5])[CH3:2].[F:22][C:23]1[CH:24]=C(N)[CH:26]=[CH:27][C:28]=1[N:29]1CCOCC1.CCN=C=NCCCN(C)C.C1C=CC2N(O)N=NC=2C=1.[CH3:57][N:58]1[CH2:63][CH2:62][O:61][CH2:60][CH2:59]1>CN(C=O)C.O>[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[CH:8][C:9]([C:12]2[CH:13]=[C:14]([C:19](=[O:21])[NH:29][C:28]3[CH:27]=[CH:26][C:57]([N:58]4[CH2:63][CH2:62][O:61][CH2:60][CH2:59]4)=[CH:24][C:23]=3[F:22])[CH:15]=[CH:16][C:17]=2[Cl:18])=[CH:10][CH:11]=1)=[O:5])[CH3:2]

Komponenten

8

Versuchsvorschrift

A mixture of 6-chloro-biphenyl-3,4′-dicarboxylic acid 4′-ethyl ester (213 mg), 3-fluoro-4-morpholin-4-yl-phenylamine (179 mg), EDAC (174 mg), HOBT (123 mg) and N-methylmorpholine (200 μl) in DMF (3 ml) was stirred at room temperature. After 11 h, water (30 ml) was added and the resulting suspension filtered. The residue was then purified by chromatography. Elution with 1:1 ethyl acetate:petrol gave a brown oil (235 mg).

Aufarbeitung

  1. filtrationthe resulting suspension filtered
  2. customThe residue was then purified by chromatography
  3. washElution with 1:1 ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-2a74595c25314e6dad8db0b72a887e34
Quelldatensatz
uspto-grants-2011_08
Patentnummer
US08008303B2

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