The development of a novel solid phase synthesis of some 5-aminopyrazoles and derivatives is described. Reaction of hydrazines with solid supported p-keto-nitrile (1) affords 5-aminopyrazoles (2) the amino group of which is readily acylated or sulphonylated. Generation of the solid supported 13-keto
Solid phase synthesis of 5-aminopyrazoles and derivatives part II
โ Scribed by Richard D. Wilson; Stephen P. Watson; Stephen A. Richards
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 196 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
A new synthesis of 5-amino pyrazoles on a solid support via in situ generation of a resin bound aldehyde nitrile is described. The synthesis is more versatile and efficient than the method that we had previously descdbed and the new route yields complementary structures.
๐ SIMILAR VOLUMES
The solid phase synthesis of 1,4-benzothiazepin-5-one derivatives, resulting from the reaction of resin-bound protected cysteine with 2-fluoro-5-nitro-benzoic acid followed by a reductive aikylation and an intra molecular cyclization, is described.
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