Ethanesulfonylchloride, 2-chloro- → HCID 66747700, Verbindung

HRID 1405829Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1405829
[H-].[Na+].Cl[CH2:4][CH2:5][S:6](Cl)(=[O:8])=[O:7].[F:10][C:11]1[CH:31]=[CH:30][C:14]([O:15][C:16]2[CH:21]=[CH:20][C:19]([C:22]3[C:23]([NH2:29])=[N:24][CH:25]=[C:26]([CH3:28])[CH:27]=3)=[CH:18][CH:17]=2)=[CH:13][C:12]=1[O:32][CH3:33]>C1COCC1>[F:10][C:11]1[CH:31]=[CH:30][C:14]([O:15][C:16]2[CH:17]=[CH:18][C:19]([C:22]3[C:23]4=[N:29][S:6](=[O:8])(=[O:7])[CH2:5][CH2:4][N:24]4[CH:25]=[C:26]([CH3:28])[CH:27]=3)=[CH:20][CH:21]=2)=[CH:13][C:12]=1[O:32][CH3:33]

Komponenten

5

Edukt 3

HCID 15385Ethanesulfonylchloride, 2-chloro-HCID 24758Sodium hydrideHCID 66748403HCID 66748403, Verbindung

Produkt 1

HCID 66747700HCID 66747700, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

To a suspension of NaH (60%, 222 mg) in THF (dry) (20 mL) was added 2-chloroethanesulfonyl chloride (0.233 mL) at 0° C. and the mixture was stirred for 10 min at the same temperature. A solution of 3-(4-(4-fluoro-3-methoxyphenoxy)phenyl)-5-methylpyridin-2-amine (360 mg) in THF (dry) (20 mL) was added at 0° C. and the mixture was stirred at room temperature under nitrogen overnight. The mixture was quenched with water at 0° C. Water, EtOAc and THF were added to the mixture and the organic phase was separated. Silica-gel was added to the organic phase and the volatiles were removed in vacuo. The mixture supported on silica-gel was purified by column chromatography (silica gel, eluted with MeOH in EtOAc) and concentrated in vacuo to give 9-[4-(4-fluoro-3-methoxyphenoxy)phenyl]-7-methyl-3,4-dihydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxide as a white solid. This product was subjected to the next reaction without further purification. A part of the product was crystallized from EtOAc/IPE to give the title compound as a colorless solid.

Aufarbeitung

  1. stirringthe mixture was stirred at room temperature under nitrogen overnight
  2. customThe mixture was quenched with water at 0° C
  3. additionWater, EtOAc and THF were added to the mixture
  4. customthe organic phase was separated
  5. additionSilica-gel was added to the organic phase
  6. customthe volatiles were removed in vacuo
  7. customwas purified by column chromatography (silica gel, eluted with MeOH in EtOAc)
  8. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-5fc80ace53de40f3a0ec6918441556fd
Quelldatensatz
uspto-grants-2014_12
Patentnummer
US08916551B2

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