z-logo
Premium
The syntheses of [ 13 C 6 ] and [phenyl‐ 14 C(U)]BMS‐816336, an inhibitor of 11β‐hydroxysteroid dehydrogenase type 1, for type 2 diabetes
Author(s) -
Maxwell Brad D.
Publication year - 2017
Publication title -
journal of labelled compounds and radiopharmaceuticals
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.432
H-Index - 47
eISSN - 1099-1344
pISSN - 0362-4803
DOI - 10.1002/jlcr.3500
Subject(s) - chemistry , stereochemistry , type (biology) , dehydrogenase , enzyme , biochemistry , ecology , biology
Type 2 diabetes is a significant worldwide health problem. To support the development of BMS‐816336 as an inhibitor of 11β‐hydroxysteroid dehydrogenase type 1 for type 2 diabetes, the synthesis of carbon‐14 labeled material was required for use in metabolic profiling. [Phenyl‐ 14 C(U)]BMS‐816336 was synthesized in 8 steps and 22% radiochemical yield from commercially available [ 14 C(U)]bromobenzene. The radiochemical purity of [phenyl‐ 14 C(U)]BMS‐816336 was 100% having a specific activity of 84.4 μCi/mg or 28.8 mCi/mmol for a total of 8.9 mCi. It was also necessary to synthesize [ 13 C 6 ]BMS‐816336 for use as a liquid chromatography/mass spectrometry standard. [ 13 C 6 ]BMS‐816336 was also prepared in 8 labeled steps in 26% yield from [ 13 C 6 ]bromobenzene.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom