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Methane → 5,11-Dihydro-11-[4-(1-pyrrolidinyl)-but-2-ynyl]-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one

HRID 1084700
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1084700
[CH2:1]([N:4]1[C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=2[C:8](=[O:15])[NH:7][C:6]2[CH:16]=[CH:17][CH:18]=[N:19][C:5]1=2)[C:2]#[CH:3].[CH2:20]=O.[NH:22]1[CH2:26][CH2:25][CH2:24][CH2:23]1.C>[Cu]Cl.O1CCOCC1>[N:22]1([CH2:20][C:3]#[C:2][CH2:1][N:4]2[C:10]3[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=3[C:8](=[O:15])[NH:7][C:6]3[CH:16]=[CH:17][CH:18]=[N:19][C:5]2=3)[CH2:26][CH2:25][CH2:24][CH2:23]1
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Komponenten

7

Edukt 4

HCID 297MethaneHCID 712FormaldehydeHCID 31268PyrrolidineHCID 145520855,11-dihydro-11-(2-propynyl)-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one

Produkt 1

HCID 145520865,11-Dihydro-11-[4-(1-pyrrolidinyl)-but-2-ynyl]-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 62652
Cuprous chloride
Katalysator
HCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

The mixture of 8.5 g (0.034 mol) of 5,11-dihydro-11-(prop-2-ynyl)-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one, 50 ml of anhydrous dioxan, 1.08 g (0.036 mol) of paraformaldehyde, 2.77 g (0.039 mol) of pyrrolidine and 0.2 g of copper (I) chloride was refluxed for 1 hour with stirring and then, after cooling, evaporated down in a water jet vacuum. The residue was partitioned between water and ethylacetate, the ethylacetate solution obtained was mixed with 2 g of animal charcoal, dried over sodium sulphate, filtered and evaporated down. The residue was purified by column chromatography on silica gel using first ethyl acetate and then dichloromethane/cyclohexane/methanol/conc. ammonia 68/15/15/2 (v/v/v/v) as eluant. The crude product obtained after evaporation of the suitable eluates was recrystallised once more from ethylacetate. Yield: 1.6 g (14% of theory) of colourless crystals, m.p. 153° C.; RF 0.5 (Merck, ready-made TLC plates, silica gel 60 F-254; eluant: dichloromethane/cyclohexane/methanol/conc. ammonia 68/15/15/2 v/v/v/v).

Aufarbeitung

  1. temperaturewas refluxed for 1 hour
  2. temperatureafter cooling
  3. customevaporated down in a water jet vacuum
  4. customThe residue was partitioned between water and ethylacetate
  5. customthe ethylacetate solution obtained
  6. dry with materialdried over sodium sulphate
  7. filtrationfiltered
  8. customevaporated down
  9. customThe residue was purified by column chromatography on silica gel using first ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-25ee1265146d4252b68fddb67155b27f
Quelldatensatz
uspto-grants-1991_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05006522

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