(3,4-Dichlorophenyl)methanesulfonyl chloride → 17-cyclopropylmethyl-3-tert-butyldimethylsilyloxy-14beta-hydroxy-4,5alpha-epoxy-6alpha-(N-methyl-3,4-dichlorophenylmethanesulfonamido)morphinan

HRID 1857459Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1857459
[CH:1]1([CH2:4][N:5]2[CH2:30][CH2:29][C@:12]34[C:13]5[C:14]6[O:28][C@H:11]3[C@@H:10]([NH:31][CH3:32])[CH2:9][CH2:8][C@@:7]4([OH:33])[C@H:6]2[CH2:19][C:18]=5[CH:17]=[CH:16][C:15]=6[O:20][Si:21]([C:24]([CH3:27])([CH3:26])[CH3:25])([CH3:23])[CH3:22])[CH2:3][CH2:2]1.[Cl:34][C:35]1[CH:36]=[C:37]([CH2:42][S:43](Cl)(=[O:45])=[O:44])[CH:38]=[CH:39][C:40]=1[Cl:41]>N1C=CC=CC=1>[CH:1]1([CH2:4][N:5]2[CH2:30][CH2:29][C@:12]34[C:13]5[C:14]6[O:28][C@H:11]3[C@@H:10]([N:31]([CH3:32])[S:43]([CH2:42][C:37]3[CH:38]=[CH:39][C:40]([Cl:41])=[C:35]([Cl:34])[CH:36]=3)(=[O:45])=[O:44])[CH2:9][CH2:8][C@@:7]4([OH:33])[C@H:6]2[CH2:19][C:18]=5[CH:17]=[CH:16][C:15]=6[O:20][Si:21]([C:24]([CH3:27])([CH3:26])[CH3:25])([CH3:22])[CH3:23])[CH2:2][CH2:3]1

Komponenten

4

Edukt 2

HCID 2794622(3,4-Dichlorophenyl)methanesulfonyl chlorideHCID 5380405917-Cyclopropylmethyl-3-tert-butyldimethylsilyloxy-14beta-hydroxy-4,5alpha-epoxy-6alpha-methylaminomorphinan

Produkt 1

HCID 9122191517-cyclopropylmethyl-3-tert-butyldimethylsilyloxy-14beta-hydroxy-4,5alpha-epoxy-6alpha-(N-methyl-3,4-dichlorophenylmethanesulfonamido)morphinanAusbeute 78 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1049PyridineLösungsmittel

Versuchsvorschrift

203.9 mg of 17-cyclopropylmethyl-3-tert-butyldimethylsilyloxy-14β-hydroxy-4,5α-epoxy-6α-(methylaminomorphinan 108 obtained in reference example 91 was dissolved in 3 ml of pyridine followed by the addition of 124 mg of 3,4-dichlorophenylmethanesufonylchloride and stirring for 30 minutes at room temperature. After concentrating the reaction system, 3 ml of saturated aqueous sodium bicarbonate and 3 ml of chloroform were added to separate layers, after which the aqueous layer was extracted twice with 3 ml of chloroform. After drying with anhydrous sodium sulfate, the organic layer was concentrated to obtain the oily crude product. This was then purified with silica gel column chromatography (30 g benzene/ethyl acetate=5/1) to obtain 235.4 mg of the target compound (yield: 78%).

Aufarbeitung

  1. concentrationAfter concentrating the reaction system, 3 ml of saturated aqueous sodium bicarbonate and 3 ml of chloroform
  2. additionwere added
  3. customto separate layers
  4. extractionafter which the aqueous layer was extracted twice with 3 ml of chloroform
  5. dry with materialAfter drying with anhydrous sodium sulfate
  6. concentrationthe organic layer was concentrated
  7. customto obtain the oily crude product
  8. customThis was then purified with silica gel column chromatography (30 g benzene/ethyl acetate=5/1)

Quellen und Nachweise

ORD-Eintrag
ord-39c72da51ad04742bcea6367e2cd56a3
Quelldatensatz
uspto-grants-2000_11
Patentnummer
US06147084

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