Efficient Synthesis of Novel 3-(5-(2-Hydroxy-2-Phenylethylsulfonyl)-4- Phenyl-4H-1,2,4-Triazol-3-yl)-1,8-Naphthyridin-4(1H)-Ones

Author(s): Muggu V.S.R.K. Chaitanya, Pilli Venkateshwarlu, Pramod K. Dubey.

Journal Name: Letters in Organic Chemistry

Volume 9 , Issue 10 , 2012

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Abstract:

The reaction of 1,4-dihydro-4-oxo-1,8-naphthyridine-3-carbohydrazide (4) with substituted phenyl isothiocyanates (5) in ethanol under reflux for 30 min gave thiosemicarbazide derivatives 6, which on cyclization in 2N NaOH under refluxing conditions for 1h resulted in 3-(5-mercapto-4-phenyl-4H-1,2,4-triazol-3-yl)-1,8-naphthyridin-4(1H)-one (7). Alternatively, 7 could also be prepared from 4 through intermediacy of 8, i.e. 4 ← 8 ← 7. In another sequence of reactions, condensation of 7 with -bromoacetylbenzene (10) in DMF and K2CO3 as base at 120oC for 2h gave 3-[5-(2-oxo-2- phenyl-ethylsulfanyl)-4-phenyl-4H-[1,2,4]triazol-3-yl]-1H-[1,8]naphthyridin-4-one (11). The latter, on oxidation with H2O2 in acetic acid at 100oC for 6h resulted in 3-[5-(2-oxo-2-phenyl-ethanesulfonyl)-4-phenyl-4H-[1,2,4]triazol-3-yl]-1H- [1,8]naphthyridin-4-one (12) which on reduction with NaBH4 in methanol at RT for 30 min yielded 3-(5-(2-hydroxy-2- phenylethylsulfonyl)-4-phenyl-4H-1,2,4-triazol-3-yl)-1,8-naphthyridin-4(1H)-one (13). Alternatively, 13 could also be prepared by reducing 11 using NaBH4 in methanol at RT for 30 min giving 3-(5-(2-hydroxy-2-phenylethylthio)-4-phenyl- 4H-1,2,4-triazol-3-yl)-1,8-naphthyridin-4(1H)-one(14) followed by oxidation with H2O2 in acetic acid at 100oC for 6h.

Keywords: H2O2 (30 %), NaBH4, Naphthyridine acid hydrazide, phenyl isothiocyanates, thiosemicarbazide

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Article Details

VOLUME: 9
ISSUE: 10
Year: 2012
Page: [732 - 738]
Pages: 7
DOI: 10.2174/157017812803901944
Price: $65

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