Synthesis of Long-chain 1-Alkylimidazole-2-thiols, 1-Alkylimidazoles, and Some Related Benzimidazole Compounds
✍ Scribed by Bäuerlein, Edmund ;Trasch, Heinz
- Book ID
- 102899627
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- English
- Weight
- 521 KB
- Volume
- 1979
- Category
- Article
- ISSN
- 0947-3440
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✦ Synopsis
Abstract
This article describes the synthesis of long‐chain 1‐alkylimidazole‐2‐thiols 3 and 1‐decylbenzimidazole‐2‐thiol (10), of value as nucleophilic scavengers for sulfenyl groups (RS^+^) in lipophilic membranes^2)^ and as inhibitors of thyroid peroxidase^3)^, as well as of the corresponding 1‐alkylimidazoles 6 and ‐benzimidoles 7. Because 1‐decyl compounds belonging to the benzimidazole series apparently have a specific action on proton translocation in the mitochondrial system, which depends on their basicity^2)^., the half‐neutralisation potentials of 7c, 10 and 11 have been determined in aqueous acetonitrile.
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## Abstract 1,1′‐Thiobis (2‐hydroxyethane) has been synthesized isotopically labelled with sulphur‐35, carbon‐13 and deuterium. The conversion to 1,1′‐thiobis (2‐chloroethane) labelled with sulphur‐35 and carbon‐13 is described.