ChemInform Abstract: O‐NITROANILINE DERIVATIVES. PART V. CYCLISATION OF N‐ACYLATED DERIVATIVES OF N‐BENZYL‐ AND N‐P‐NITROBENZYL‐O‐NITROANILINE‐ A COMPARISON OF CARBOXAMIDES AND SULPHONAMIDES

Machin, J.; Mackie, R. K.; McNab, Hamish; Reed, Gerald.; Sagar, Anthony J. G.; Smith, David M.

doi:10.1002/chin.197619248

Chemischer Informationsdienst

1976

DOI: 10.1002/chin.197619248

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ChemInform Abstract: O‐NITROANILINE DERIVATIVES. PART V. CYCLISATION OF N‐ACYLATED DERIVATIVES OF N‐BENZYL‐ AND N‐P‐NITROBENZYL‐O‐NITROANILINE‐ A COMPARISON OF CARBOXAMIDES AND SULPHONAMIDES

J. Machin¹,

R. K. Mackie²,

Hamish McNab³

et al.

Abstract: Die Cyclisierung der N‐Nitrobenzyl‐sulfonamide (Ia), (Ib) bzw. ‐amide (Ic) mit methanolischem Na‐methylat liefert jeweils das Benzimidazol (II); nur im Falle von (Ia) wird daneben das Methylderivat (III) erhalten [im Falle von (Ib) Bildung von (III) nur in Spuren].

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ChemInform Abstract: O‐NITROANILINE DERIVATIVES. PART V. CYCLISATION OF N‐ACYLATED DERIVATIVES OF N‐BENZYL‐ AND N‐P‐NITROBENZYL‐O‐NITROANILINE‐ A COMPARISON OF CARBOXAMIDES AND SULPHONAMIDES

Abstract: Die Cyclisierung der N‐Nitrobenzyl‐sulfonamide (Ia), (Ib) bzw. ‐amide (Ic) mit methanolischem Na‐methylat liefert jeweils das Benzimidazol (II); nur im Falle von (Ia) wird daneben das Methylderivat (III) erhalten [im Falle von (Ib) Bildung von (III) nur in Spuren].

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