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http://nopr.niscpr.res.in/handle/123456789/15197Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Sekharayya, M Chandra | - |
| dc.contributor.author | Narayana, G Venkata | - |
| dc.contributor.author | Nigam, Satish | - |
| dc.contributor.author | Madhusudhan, G | - |
| dc.date.accessioned | 2012-12-08T15:54:14Z | - |
| dc.date.available | 2012-12-08T15:54:14Z | - |
| dc.date.issued | 2012-12 | - |
| dc.identifier.issn | 0975-0983(Online); 0376-4699(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/15197 | - |
| dc.description | 1763-1766 | en_US |
| dc.description.abstract | An improved and scalable method is developed for the synthesis of 7-ethyltryptophol, a key intermediate for Etodolac, a non-steroidal anti-inflammatory drug (NSAID) starting from commercially available 2-ethylphenyl hydrazine and dihydrofuran with H2SO4 as a catalyst in N,N-dimethylacetamide (DMAc)-H2O (1:1) as a solvent in 69% yield. The method is easy, inexpensive and reproducible and the process is clean, high yielding and operationally simple. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | NISCAIR-CSIR, India | en_US |
| dc.rights | CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
| dc.source | IJC-B Vol.51B(12) December 2012] | en_US |
| dc.subject | Etodolac | en_US |
| dc.subject | 7-Ethyltryptophol | en_US |
| dc.subject | 2-Ethylphenyl¬hydrazine hydrochloride | en_US |
| dc.subject | Anti-inflammatory drug N,N-dimethylacetamide | en_US |
| dc.title | An improved and scalable process for the synthesis of a key intermediate for Etodolac, a non-steroidal anti-inflammatory drug | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.51B(12) December 2012] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 51B(12) 1763-1766.pdf | 64.7 kB | Adobe PDF | View/Open |
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