Novel compounds for the synthesis of cefdinir
✍ Scribed by K. V. V. Prasada Rao; Ramesh Dandala; Meenakshisunderam Sivakumaran; Ananta Rani; A. Naidu
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2007
- Tongue
- English
- Weight
- 417 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
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Preparation of two new compounds 2‐mercapto‐5‐methyl‐1,3,4‐thiadiazolyl‐(Z)‐2‐(2‐amino‐4‐thiazolyl)‐2‐trityloxyiminoacetate (14) and 2‐mercapto‐5‐methyl‐1, 3,4‐thiadiazolyl‐ (Z)‐2‐(2‐amino‐4‐thiazolyl)‐2‐acetyloxyiminoacetate (12) and their use in the preparation of 7β‐[(Z)‐2‐(2‐amino‐4‐thiazolyl)‐2‐hydroxyiminoacetamido]‐3‐vinylcephem‐4‐carboxylic acid, also known by the generic name Cefdinir (1) has been accomplished in a single step by coupling with 7‐amino‐3‐vinylcephem‐4‐carboxylic acid (7) with purity of greater than 99% by HPLC.
📜 SIMILAR VOLUMES
Novel fused heterotricyclic compounds 3-6 containing two different dipyrazolopyrimidine framework were prepared from 1a-1d. The reaction of 1 with K 2 CO 3 in DMSO or NaH in DMF led to the formation of 2 or 3, respectively, which reacted further to afford 6 or 5, respectively.