1980Journal of Heterocyclic ChemistryRequires access

Polycondensed nitrogen heterocycles. IX. 5,6‐dihydro‐7H‐pyrrolo[1,2‐d][1,4]benzodiazepin‐6‐one

Gaetano Dattolo, Girolamo Cirrincione, Enrico Aiello

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Abstract

Abstract The reaction of amino derivative I with bromoacetyl bromide led to the formation of a complex mixture from which, in addition to the title compound, which was formed in low yield, compounds III, IV and VI were separated. Pyrrolo[1,2‐d][1,4]benzodiazepine V was obtained in 85% yield when the bromoamide III was treated with an equimolar amount of potassium t‐butoxide.

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Abstract The reaction of amino derivative I with bromoacetyl bromide led to the formation of a complex mixture from which, in addition to the title compound, which was formed in low yield, compounds III, IV and VI were separated. Pyrrolo[1,2‐d][1,4]benzodiazepine V was obtained in 85% yield when the bromoamide III was treated with an equimolar amount of potassium t‐butoxide.

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Available abstract

Abstract The reaction of amino derivative I with bromoacetyl bromide led to the formation of a complex mixture from which, in addition to the title compound, which was formed in low yield, compounds III, IV and VI were separated. Pyrrolo[1,2‐d][1,4]benzodiazepine V was obtained in 85% yield when the bromoamide III was treated with an equimolar amount of potassium t‐butoxide.

Key concepts: Chemistry, Yield (engineering), Bromide, Potassium bromide, Derivative (finance), Potassium, Medicinal chemistry, Nitrogen

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Polycondensed nitrogen heterocycles. IX. 5,6‐dihydro‐7H‐pyrrolo[1,2‐d][1,4]benzodiazepin‐6‐one — Research Paper | ScholarLens