Dergiler / Turkish Journal of Chemistry / 2004 / Cilt: 28 - Sayı: 6

Synthesis and Antitumor Activities of Some New 4-(1-Naphthylidenamino)- and 4-(1-Naphthylmethylamino)-1,2,4-Triazol-5-one Derivatives

Sayfa
679–690
Yayın Tarihi
2004-06-01
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

The in vitro antitumor activities of some selected compounds were screened and compounds 3e, 5c, 6e and 9c} were found to be active.

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Amaç & Hipotez:A series of 4-(1-naphthylidenamino)-1,2,4-triazol-5-one derivatives (3a-e) were synthesized by condensation of corresponding 3-alkyl-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones with 1-naphthaldehyde.
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Temel Bulgular & Veri:Acetylation and alkylation of these compounds gave 4a-e and 5a-e, respectively.
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Sonuç & Katkı:The in vitro antitumor activities of some selected compounds were screened and compounds 3e, 5c, 6e and 9c} were found to be active.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:4-triazol-5-one · 1-naphthaldehyde · Acetylation

Özet

A series of 4-(1-naphthylidenamino)-1,2,4-triazol-5-one derivatives (3a-e) were synthesized by condensation of corresponding 3-alkyl-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones with 1-naphthaldehyde. Acetylation and alkylation of these compounds gave 4a-e and 5a-e, respectively. Sodium borohydride reduction of 1-naphthylidenamino derivatives afforded naphthylmethylamino derivatives, which were subsequently acetylated. Depending on the duration of the acetylation, mono or bis acetamide derivatives were obtained. The in vitro antitumor activities of some selected compounds were screened and compounds 3e, 5c, 6e and 9c} were found to be active.

Abstract

A series of 4-(1-naphthylidenamino)-1,2,4-triazol-5-one derivatives (3a-e) were synthesized by condensation of corresponding 3-alkyl-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones with 1-naphthaldehyde. Acetylation and alkylation of these compounds gave 4a-e and 5a-e, respectively. Sodium borohydride reduction of 1-naphthylidenamino derivatives afforded naphthylmethylamino derivatives, which were subsequently acetylated. Depending on the duration of the acetylation, mono or bis acetamide derivatives were obtained. The in vitro antitumor activities of some selected compounds were screened and compounds 3e, 5c, 6e and 9c} were found to be active.

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Bu Makaleye Atıf Yap

DEMİRBAŞ, N., UĞURLUOĞLU, R. (2004). Synthesis and Antitumor Activities of Some New 4-(1-Naphthylidenamino)- and 4-(1-Naphthylmethylamino)-1,2,4-Triazol-5-one Derivatives. Turkish Journal of Chemistry, Cilt: 28 - Sayı: 6, 679–690. https://ajindex.com/articles/185366

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