Benzenesulfonyl chloride → HCID 67243254, Verbindung

HRID 2421882

Reaktionsgleichung

Reaktionsgleichung von HRID 2421882
[NH:1]1[CH2:6][CH2:5][O:4][C:3]2[N:7]=[CH:8][C:9]([C:11]([O:13][CH3:14])=[O:12])=[CH:10][C:2]1=2.[C:15]1([S:21](Cl)(=[O:23])=[O:22])[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.CCN(C(C)C)C(C)C>C(Cl)Cl.CN(C1C=CN=CC=1)C>[C:15]1([S:21]([N:1]2[CH2:6][CH2:5][O:4][C:3]3[N:7]=[CH:8][C:9]([C:11]([O:13][CH3:14])=[O:12])=[CH:10][C:2]2=3)(=[O:23])=[O:22])[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1

Komponenten

6

Edukt 3

HCID 7369Benzenesulfonyl chlorideHCID 81531DiisopropylethylamineHCID 57896765methyl 2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine-7-carboxylate

Produkt 1

HCID 67243254HCID 67243254, VerbindungAusbeute 58,3 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 142844-(Dimethylamino)pyridineKatalysatorHCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

To a solution of methyl 2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine-7-carboxylate (278.9 mg, 1.436 mmol) in DCM (20 mL) was added benzenesulfonyl chloride (278 μL, 2.156 mmol), DIPEA (753 μL, 4.31 mmol) and DMAP (88 mg, 0.719 mmol). The reaction was stirred at room temperature for 16 hours. LCMS analysis indicated a predominance of product in the reaction mixture. The solvent was removed under reduced pressure and the resulting oil was purified by flash column chromatography using a gradient elution of hexanes with 25-70% EtOAc to provide methyl 1-(phenylsulfonyl)-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine-7-carboxylate (280 mg, 0.837 mmol, 58.3% yield) as a yellow glass. LCMS (+ESI) m/z=334.8 [M+H]+.

Aufarbeitung

  1. customThe solvent was removed under reduced pressure
  2. customthe resulting oil was purified by flash column chromatography
  3. washa gradient elution of hexanes with 25-70% EtOAc

Quellen und Nachweise

ORD-Eintrag
ord-259e3c5dacc54c7486c88b5c0ca2d180
Quelldatensatz
uspto-grants-2011_06
Patentnummer
US07960377B2

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