Triethylamine → Furan-2-carboxylic acid [2-methyl-3'-(4-morpholin-4-yl-phenylcarbamoyl)-biphenyl-4-yl]-amide

HRID 1678460Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1678460
[N:1]1([C:7]2[CH:12]=[CH:11][C:10]([NH:13][C:14]([C:16]3[CH:17]=[C:18]([C:22]4[CH:27]=[CH:26][C:25]([NH2:28])=[CH:24][C:23]=4[CH3:29])[CH:19]=[CH:20][CH:21]=3)=[O:15])=[CH:9][CH:8]=2)[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.C(N(CC)CC)C.[O:37]1[CH:41]=[CH:40][CH:39]=[C:38]1[C:42](Cl)=[O:43]>CN(C=O)C>[CH3:29][C:23]1[CH:24]=[C:25]([NH:28][C:42]([C:38]2[O:37][CH:41]=[CH:40][CH:39]=2)=[O:43])[CH:26]=[CH:27][C:22]=1[C:18]1[CH:19]=[CH:20][CH:21]=[C:16]([C:14](=[O:15])[NH:13][C:10]2[CH:9]=[CH:8][C:7]([N:1]3[CH2:6][CH2:5][O:4][CH2:3][CH2:2]3)=[CH:12][CH:11]=2)[CH:17]=1

Komponenten

5

Versuchsvorschrift

A solution of 4′-amino-2′-methyl-biphenyl-3-carboxylic acid (4-morpholin-4-yl-phenyl)-amide (40 mg) and triethylamine (0.4 ml) in dry DMF (3 ml) was treated with furan-2-carbonyl chloride (0.015 ml) and the mixture stirred at 20 C for 18 h. The mixture was then partitioned between water and dichloromethane. The dried extract was then evaporated and the residue purified on silica gel. Elution with dichloromethane:ethanol:0.880 ammonia; 400:8:1 gave a colourless foam (46 mg).

Aufarbeitung

  1. customThe mixture was then partitioned between water and dichloromethane
  2. extractionThe dried extract
  3. customwas then evaporated
  4. customthe residue purified on silica gel
  5. washElution with dichloromethane

Quellen und Nachweise

ORD-Eintrag
ord-ff18a3670f254a9188c057238b9529d7
Quelldatensatz
uspto-grants-2011_08
Patentnummer
US08008303B2

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