Cyclopropylamine → HCID 58930836, Verbindung

HRID 387940

Reaktionsgleichung

Reaktionsgleichung von HRID 387940
[F:1][C:2]1[CH:33]=[CH:32][C:5]([NH:6][C:7]([NH:9][C:10]2[CH:31]=[CH:30][C:13]([O:14][C:15]3[C:24]4[C:19](=[CH:20][C:21]([O:28][CH3:29])=[C:22]([C:25](O)=[O:26])[CH:23]=4)[N:18]=[CH:17][CH:16]=3)=[CH:12][CH:11]=2)=[O:8])=[CH:4][CH:3]=1.Cl.C(N=C=N[CH2:40][CH2:41][CH2:42][N:43](CC)CC)C.O.ON1C2C=CC=CC=2N=N1.C1(N)CC1>CN(C)C=O.O.C(OCC)(=O)C.C(N(CC)CC)C>[CH:42]1([NH:43][C:25]([C:22]2[CH:23]=[C:24]3[C:19](=[CH:20][C:21]=2[O:28][CH3:29])[N:18]=[CH:17][CH:16]=[C:15]3[O:14][C:13]2[CH:30]=[CH:31][C:10]([NH:9][C:7]([NH:6][C:5]3[CH:32]=[CH:33][C:2]([F:1])=[CH:3][CH:4]=3)=[O:8])=[CH:11][CH:12]=2)=[O:26])[CH2:40][CH2:41]1

Komponenten

9

Edukt 4

HCID 69828CyclopropylamineHCID 27960291-Hydroxybenzotriazole hydrateHCID 99645121-(3-Diethylaminopropyl)-3-ethylcarbodiimide hydrochlorideHCID 229363504-(4-(((4-Fluoroanilino)carbonyl)amino)phenoxy)-7-methoxy-6-quinolinecarboxylic acid

Produkt 1

HCID 58930836HCID 58930836, VerbindungAusbeute 44,5 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 962WaterLösungsmittelHCID 6228DimethylformamideLösungsmittelHCID 8471TriethylamineLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

After dissolving the N-[4-(6-carboxy-7-methoxy-4-quinolyl)oxyphenyl]-N′-(4-fluorophenyl)urea (60 mg) synthesized in Example 341 in dimethylformamide (1.5 ml), there were added 1-ethyl-3-(3-diethylaminopropyl)-carbodiimide hydrochloride (39 mg), 1-hydroxy-1H-benzotriazole monohydrate (31 mg), triethylamine (30 μl) and cyclopropylamine (0.05 ml) and the mixture was stirred overnight at room temperature. The reaction solution was distributed between ethyl acetate and water, and the organic layer was washed with water and then dried over anhydrous sodium sulfate. After distilling off the solvent, crystals were precipitated with ethyl acetate, filtered out and dried under reduced pressure to obtain the title compound (29 mg) as white crystals.

Aufarbeitung

  1. washthe organic layer was washed with water
  2. dry with materialdried over anhydrous sodium sulfate
  3. distillationAfter distilling off the solvent, crystals
  4. customwere precipitated with ethyl acetate
  5. filtrationfiltered out
  6. customdried under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-3420ff75cd274140a16e1c02037ed533
Quelldatensatz
uspto-grants-2013_02
Patentnummer
US08372981B2

Verknüpfte Notizen

Wird geladen…