The synthesis of pyrrolo[2,1-d][1,2,5]benzothiadiazepin-7(6H)-one 5,5-dioxide has been achieved by reaction between 2-(1H-pyrrol-1-yl)benzenesulfonamide and triphosgene. N-Ethylation of the tricyclic derivative afforded 6-ethylpyrrolo[2,1-d][1,2,5]benzothiadiazepin-7(6H)-one 5,5-dioxide, also obtained by the action of trifosgene on N-ethyl 2-(1H-pyrrol-1-yl)benzenesulfonamide. Preparation of pyrrole derivatives from 2-aminobenzenesulfonamide and its N-ethyl derivative by Clauson-Kaas procedure required preliminary protection of the sulfonamide function.

Heterocycles with a benzothiadiazepine moiety .5. Derivatives of pyrrolo[2,1-d][1,2,5]benzothiadiazepine, a novel tricyclic ring / DI SANTO, Roberto; Costi, Roberta; Marino, Artico; Silvio, Massa. - In: IL FARMACO. - ISSN 0014-827X. - STAMPA. - 52:6-7(1997), pp. 375-378.

Heterocycles with a benzothiadiazepine moiety .5. Derivatives of pyrrolo[2,1-d][1,2,5]benzothiadiazepine, a novel tricyclic ring

DI SANTO, Roberto;COSTI, Roberta;
1997

Abstract

The synthesis of pyrrolo[2,1-d][1,2,5]benzothiadiazepin-7(6H)-one 5,5-dioxide has been achieved by reaction between 2-(1H-pyrrol-1-yl)benzenesulfonamide and triphosgene. N-Ethylation of the tricyclic derivative afforded 6-ethylpyrrolo[2,1-d][1,2,5]benzothiadiazepin-7(6H)-one 5,5-dioxide, also obtained by the action of trifosgene on N-ethyl 2-(1H-pyrrol-1-yl)benzenesulfonamide. Preparation of pyrrole derivatives from 2-aminobenzenesulfonamide and its N-ethyl derivative by Clauson-Kaas procedure required preliminary protection of the sulfonamide function.
1997
"aids-hiv"; hiv non-nucleoside reverse transcriptase inhibitors
01 Pubblicazione su rivista::01a Articolo in rivista
Heterocycles with a benzothiadiazepine moiety .5. Derivatives of pyrrolo[2,1-d][1,2,5]benzothiadiazepine, a novel tricyclic ring / DI SANTO, Roberto; Costi, Roberta; Marino, Artico; Silvio, Massa. - In: IL FARMACO. - ISSN 0014-827X. - STAMPA. - 52:6-7(1997), pp. 375-378.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/245204
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