Dimethyl Sulfoxide → HCID 59427282, Verbindung

HRID 503556Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 503556
Cl[C:2]1[C:11]2[C:6](=[CH:7][C:8]([C:12]#[N:13])=[CH:9][CH:10]=2)[N:5]=[CH:4][CH:3]=1.[CH2:14]([C:16]1[CH:21]=[C:20]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[N:19]=[N:18][C:17]=1[NH:28][C:29]1[CH:34]=[CH:33][C:32]([OH:35])=[CH:31][CH:30]=1)[CH3:15].C(=O)([O-])[O-:37].[Cs+].[Cs+].CS(C)=O>O>[CH2:14]([C:16]1[CH:21]=[C:20]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[N:19]=[N:18][C:17]=1[NH:28][C:29]1[CH:30]=[CH:31][C:32]([O:35][C:2]2[C:11]3[C:6](=[CH:7][C:8]([C:12]([NH2:13])=[O:37])=[CH:9][CH:10]=3)[N:5]=[CH:4][CH:3]=2)=[CH:33][CH:34]=1)[CH3:15]

Komponenten

6

Versuchsvorschrift

A microwave reaction vial was charged with 4-chloroquinoline-7-carbonitrile (97.1 mg, 0.515 mmol), 4-(4-ethyl-6-phenylpyridazin-3-ylamino)phenol (150 mg, 0.515 mmol), cesium carbonate (252 mg, 0.772 mmol) and 2.6 mL of DMSO. The vial was sealed, and the reaction mixture was irradiated in the microwave at 150° C. for 15 min. Upon cooling the mixture was poured into water and the resulting solids were filtered and washed with water. The crude solids were dissolved in 90/10/1 CH2Cl2/MeOH/NH4OH and purified by silica gel chromatography, 5-100% 90/10/1: CH2Cl2 over 25 min which provided 4-(4-(4-ethyl-6-phenylpyridazin-3-ylamino)phenoxy)quinoline-7-carboxamide as a tan solid. MS m/z=462 [M+H]+. Calc'd for C28H23N3O2: 461.52.

Aufarbeitung

  1. customA microwave reaction
  2. customThe vial was sealed
  3. customthe reaction mixture was irradiated in the microwave at 150° C. for 15 min
  4. temperatureUpon cooling the mixture
  5. filtrationthe resulting solids were filtered
  6. washwashed with water
  7. dissolutionThe crude solids were dissolved in 90/10/1 CH2Cl2/MeOH/NH4OH
  8. custompurified by silica gel chromatography, 5-100% 90/10/1

Quellen und Nachweise

ORD-Eintrag
ord-072ff22ac1704e6691d60824e9b999c2
Quelldatensatz
uspto-grants-2010_08
Patentnummer
US07776857B2

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