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    New Sulfamides Based on 1-Izopropil-3-Ξ±-Naftyl-5- Methoxymethyl-4-Aminopyrazole and Determination of Their Structure

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    Для Ρ€Π°Π½Π΅Π΅ ΠΏΠΎΠ»ΡƒΡ‡Π΅Π½Π½ΠΎΠ³ΠΎ 1-ΠΈΠ·ΠΎΠΏΡ€ΠΎΠΏΠΈΠ»-3-Ξ±-Π½Π°Ρ„Ρ‚ΠΈΠ»-5-мСтоксимСтил-4-Π½ΠΈΡ‚Ρ€ΠΎΠ·ΠΎΠΏΠΈΡ€Π°Π·ΠΎΠ»Π° ΠΏΡ€ΠΎΠ²Π΅Π΄Π΅Π½Π° рСакция восстановлСния Π³ΠΈΠ΄Ρ€Π°Π·ΠΈΠ½Π³ΠΈΠ΄Ρ€Π°Ρ‚ΠΎΠΌ. Π’ΠΏΠ΅Ρ€Π²Ρ‹Π΅ Π±Ρ‹Π» синтСзирован 1-ΠΈΠ·ΠΎΠΏΡ€ΠΎΠΏΠΈΠ»-3-Ξ±-Π½Π°Ρ„Ρ‚ΠΈΠ»-5-мСтоксимСтил-4-Π°ΠΌΠΈΠ½ΠΎΠΏΠΈΡ€Π°Π·ΠΎΠ», ΠΊΠΎΡ‚ΠΎΡ€Ρ‹ΠΉ Π·Π°Ρ‚Π΅ΠΌ ΡΡƒΠ»ΡŒΡ„ΠΎΠ½ΠΈΠ»ΠΈΡ€ΠΎΠ²Π°Π»ΠΈ ΠΏ-Π°Ρ†Π΅Ρ‚Π°ΠΌΠΈΠ΄ΠΎΠ±Π΅Π½Π·ΠΎΠ»ΡΡƒΠ»ΡŒΡ„ΠΎΡ…Π»ΠΎΡ€ΠΈΠ΄ΠΎΠΌ ΠΈ ΠΏ-Ρ‚ΠΎΠ»ΡƒΠΎΠ»ΡΡƒΠ»ΡŒΡ„ΠΎΡ…Π»ΠΎΡ€ΠΈΠ΄ΠΎΠΌ. Π’ Ρ€Π΅Π·ΡƒΠ»ΡŒΡ‚Π°Ρ‚Π΅ ΠΏΠΎΠ»ΡƒΡ‡Π΅Π½Ρ‹ Ρ€Π°Π½Π΅Π΅ нСизвСстныС ΡΡƒΠ»ΡŒΡ„ΠΎΠ½ΠΈΠ»ΠΈΡ€ΠΎΠ²Π°Π½Π½Ρ‹Π΅ ΠΏΡ€ΠΎΠΈΠ·Π²ΠΎΠ΄Π½Ρ‹Π΅ N-Π°Π»ΠΊΠΈΠ»ΠΈΡ€ΠΎΠ²Π°Π½Π½Ρ‹Ρ… Π°ΠΌΠΈΠ½ΠΎΠΏΠΈΡ€Π°Π·ΠΎΠ»ΠΎΠ². Бостав ΠΈ строСниС ΠΏΠΎΠ΄Ρ‚Π²Π΅Ρ€ΠΆΠ΄Π΅Π½Ρ‹ соврСмСнными ΠΌΠ΅Ρ‚ΠΎΠ΄Π°ΠΌΠΈ Π°Π½Π°Π»ΠΈΠ·Π°, Ρ‚Π°ΠΊΠΈΠΌΠΈ ΠΊΠ°ΠΊ ИК-, ЯМР 1Н-спСктроскопия ΠΈ масс-спСктромСтрияFor the previously obtained 1-isopropyl-3-Ξ±-naphthyl-5-methoxymethyl-4-nitrosopyrazole, a reduction reaction with hydrazine hydrate was performed. It was first synthesized by 1-isopropyl-3-Ξ±-naphthyl- 5-methoxymethyl-4-aminopyrazole which was then sulfonylated by p-acetamidobenzenesulfonyl chloride and p-toluenesulfonic chloride. As a result previously unknown sulfonylated derivatives of N-alkylated aminopyrazoles were obtained. The composition and structure are confirmed by modern methods of analysis such as IR, 1H NMR spectroscopy and mass spectrometr
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