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‘One-pot’ nitro reduction–cyclisation solid phase route to benzimidazoles

✍ Scribed by Zemin Wu; Philip Rea; Geoffrey Wickham


Publisher
Elsevier Science
Year
2000
Tongue
French
Weight
65 KB
Volume
41
Category
Article
ISSN
0040-4039

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✦ Synopsis


An improved solid phase synthesis of benzimidazoles is described. A polymer-bound o-nitroaniline was reacted with aldehydes in DMF in the presence of SnCl 2 •2H 2 O at 60°C for three hours to give benzimidazoles in excellent purity and good yield after TFA cleavage. A library of 25 benzimidazoles was prepared using this 'one-pot' procedure.