참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Ammonium Hydroxide | HCID 14923 | — |
| 반응물 | 3-[3-(5-Bromo-3-methylpyrid-2-yl)propyl]-6-(3-pyridylmethyl)-3H-1,2,3-triazolo[5,4-b]pyridine | HCID 19851790 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | HCID 19851783 | HCID 19851783 | — |
반응 단계
3-[3-(5-Bromo-3-methylpyrid-2-yl)propyl]-6-(3-pyridylmethyl)-3H-1,2,3-triazolo[5,4-b]pyridine (2.68 g) was added in portions over 15 minutes to hot (190°-200° C.) stirred polyphosphoric acid (10.45 g). The stirred reaction was heated at 190°-200° C. for a further 45 minutes, water (20 ml) was added to the hot reaction mixture, the solution was neutralised with concentrated ammonium hydroxide and allowed to cool. The pH was then raised to 10, chloroform extraction of the aqueous mixture gave a brown solid. This solid was recrystallised from ethanol/ether giving buff crystals (1.64 g). These were chromatographed on silica in methanol/chloroform 1:9, the product was then recrystallised from chloroform/petroleum ether (40°-60° C.) to give the title compound (1.4 g) (off-white crystals), m.p. 141°-143° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04764519 |
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| 출처 데이터셋 | uspto-grants-1988_08 |
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| ORD ID | ord-e01fb21c2c1144d38adac2354ac31156 |
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| 출처 메모 | uspto-grants-1988_08 |
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