Triphenylphosphine → N-[(4-chlorophenyl)methyl]-1-(2-ethylsulfanylethyl)-6-(morpholinomethyl)-4-oxo-quinoline-3-carboxamide

HRID 1068003Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1068003
[Cl:1][C:2]1[CH:29]=[CH:28][C:5]([CH2:6][NH:7][C:8]([C:10]2[CH:11]=[N:12][C:13]3[C:18]([C:19]=2[OH:20])=[CH:17][C:16]([CH2:21][N:22]2[CH2:27][CH2:26][O:25][CH2:24][CH2:23]2)=[CH:15][CH:14]=3)=[O:9])=[CH:4][CH:3]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C([CH:51](O)[CH2:52][S:53][CH2:54][CH:55](O)CC)C.N(C(OCC)=O)=NC(OCC)=O>C1COCC1>[Cl:1][C:2]1[CH:29]=[CH:28][C:5]([CH2:6][NH:7][C:8]([C:10]2[C:19](=[O:20])[C:18]3[C:13](=[CH:14][CH:15]=[C:16]([CH2:21][N:22]4[CH2:23][CH2:24][O:25][CH2:26][CH2:27]4)[CH:17]=3)[N:12]([CH2:51][CH2:52][S:53][CH2:54][CH3:55])[CH:11]=2)=[O:9])=[CH:4][CH:3]=1

Komponenten

6

Versuchsvorschrift

A dry flask containing N-(4-chlorobenzyl)-4-hydroxy-6-(4-morpholinylmethyl)-3-quinolinecarboxamide (0.20 gm) from Preparation No. 40 in dry THF (5 mL) under an argon atmosphere is added triphenylphosphine (393 mg), ethyl 2-hydroxyethylsulfide (0.16 mL) and diethyl azodicarboxylate (0.18 mL). The mixture is stirred at room temperature overnight then concentrated under reduced pressure. The crude product is purified by flash column chromatography eluting with 2% to 6% methanol in dichloromethane and then by recrystallization from ethanolcyclohexane to afford 0.21 gm of the title compound as a white solid.

Aufarbeitung

  1. customfrom Preparation No
  2. concentrationthen concentrated under reduced pressure
  3. customThe crude product is purified by flash column chromatography
  4. washeluting with 2% to 6% methanol in dichloromethane
  5. customby recrystallization from ethanolcyclohexane

Quellen und Nachweise

ORD-Eintrag
ord-94118e7b87a449688e80c0a1c478192c
Quelldatensatz
uspto-grants-2001_06
Patentnummer
US06248739B1

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