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HRID 268169Erstellt: 25. Oktober 2026

10-methyl-2,3-dihydro-1H-pyrrolo[2,1-c][1,4]benzodiazepine-5,11(10H,11aH)-dione → 8-Chloro-1,2,3,5,10,11a-hexahydro-10-methyl-11 H-pyrrolo[2,1-c] [1,4] benzodiazepin-11-one

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Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt10-methyl-2,3-dihydro-1H-pyrrolo[2,1-c][1,4]benzodiazepine-5,11(10H,11aH)-dioneHCID 9859436—
Edukt(+)-8-chloro-1,2,3,11 a-tetrahydro-10-methyl-5 H-pyrrolo[2,1-c] [1,4] benzodiazepin-5,11(10H)-dioneHCID 68145444—
Produkt8-Chloro-1,2,3,5,10,11a-hexahydro-10-methyl-11 H-pyrrolo[2,1-c] [1,4] benzodiazepin-11-oneHCID 68146023—

Reaktionsschritte

This compound is obtained when (+)-8-chloro-1,2,3,11 a-tetrahydro-10-methyl-5 H-pyrrolo[2,1-c] [1,4] benzodiazepin-5,11(10H)-dione (melting point 191° -194°C. prepared from L-proline and 4-chloro-N-methylisatoic anhydride is described in Example 1) is substituted for (+) 1,2,3,11a-tetrahydro-10 -methyl-5 H-pyrrolo[2,1-c] [1,4] benzodiazepin-5,11(10H)-dione in the process of Example 1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03947408
Quelldatensatzuspto-grants-1976_03
ORD IDord-992412ba57cf442cb2c356e023131340
Quellennotizuspto-grants-1976_03