Methanol → 3-Methoxysulfonylamino-3-methyl-N-[2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-3(R)-yl]butanamide

HRID 1033439Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1033439
[NH2:1][C@@H:2]1[CH2:8][CH2:7][C:6]2[CH:9]=[CH:10][CH:11]=[CH:12][C:5]=2[NH:4][C:3]1=[O:13].C(N(CC)CC)C.Cl[S:22]([N:25]1[C:28]([CH3:30])([CH3:29])[CH2:27][C:26]1=[O:31])(=[O:24])=[O:23].[CH3:32][OH:33]>>[CH3:32][O:33][S:22]([NH:25][C:28]([CH3:30])([CH3:29])[CH2:27][C:26]([NH:1][C@@H:2]1[CH2:8][CH2:7][C:6]2[CH:9]=[CH:10][CH:11]=[CH:12][C:5]=2[NH:4][C:3]1=[O:13])=[O:31])(=[O:24])=[O:23]

Komponenten

5

Edukt 4

HCID 887Methanol3×HCID 8471TriethylamineHCID 10103689(R)-3-amino-4,5-dihydro-1H-benzo[b]azepin-2(3H)-oneHCID 109434452,2-Dimethyl-4-oxoazetidine-1-sulfonyl chloride

Produkt 1

HCID 108615583-Methoxysulfonylamino-3-methyl-N-[2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-3(R)-yl]butanamide

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

A suspension of 98.31 g (0.530 mol) of 3(R)-amino-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one in 1600 mL of methanol at room temperature was treated with 155 mL (1.112 mol) of triethylamine. The resulting suspension was cooled to 0° C. and treated with a solution of 110.01 g (0.557 mol) of N-chlorosulfonyl-4,4-dimethylazetidin-2-one in 960 mL of methanol over 20 minutes maintaining the internal temperature below 10° C. Additional methanol (100 mL) was used to rinse the flask and the rinse was transferred into the reaction vessel. The reaction mixture was warmed to room temperature and stirred for 90 minutes.

Aufarbeitung

  1. temperaturemaintaining the internal temperature below 10° C
  2. washto rinse the flask
  3. temperatureThe reaction mixture was warmed to room temperature

Quellen und Nachweise

ORD-Eintrag
ord-f6a5ad08be6f424fbfe48ad6017e32f6
Quelldatensatz
uspto-grants-1994_05
Patentnummer
US05310737

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