Synthesis of deuterated 4,4′-diaminodiphenylsulfone (Dapsone) and related analogs
✍ Scribed by Peter M. Gannett; Edward M. Johnson II; Michael A. Grimes; Alan L. Myers; Robert E. Deavers III; Timothy S. Tracy
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- French
- Weight
- 97 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0022-2135
- DOI
- 10.1002/jlcr.649
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✦ Synopsis
Abstract
A general scheme for the synthesis of 4,4′‐diaminodiphenylsulfone‐d~5~ (Dapsone) from aniline‐d~5~ is described. The method may have general application and the preparation of the related analogs, 4,4′‐dimethylaminodiphenyl sulfone from aniline‐d~5~ and 4,4′‐dimethoxydiphenyl sulfone from phenol‐d~5~, is also described. Copyright © 2002 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
1 -Methyl-4-phenyl-2-pyridone has been used as starting material for the efficient and regioselective synthesis of deuterated analogues of the neurotoxin 1 -methyl-4-phenyl-l,2,3,6-tetrahydropyridine (MPTP). MPTP-2,242, MPTP-6,6-& and MPTP-2,2,6,6-d4 were obtained in good yield through a combination
## SYNTtIESIS AHD CHARACTERIZATION OF CARBON-14 LABELLED 4,4'-DIAMINODIPHENYL SULFONE (DAPSONE-l4C; D 3 S -1 4 C > , C.E. B l a c k b u r n and A.J. G l a z k o . D e p a r t m e n t o f P h a r m a c o l o g y . D i v i s i o n of S c i e n t i f i c and M e d i c a l Affairs. P a r k e -D a v i