Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 578087생성일: 2026년 10월 25일
1-Hydroxybenzotriazole → 5-(5-(Pyrrol-1-yl)pyridin-3-yl)-3-(pyridin-3-yl)-1,2,4-oxadiazole
https://huagongshe.com/reaction/578087
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Hydroxybenzotriazole | HCID 75771 | — |
| 반응물 | N-Hydroxynicotinimidamide | HCID 308113 | — |
| 반응물 | 5-(1H-pyrrol-1-yl)pyridine-3-carboxylic acid | HCID 2050101 | — |
| 반응물 | N-(3-methylaminopropyl)-N'-ethylcarbodiimide hydrochloride | HCID 9794023 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 5-(5-(Pyrrol-1-yl)pyridin-3-yl)-3-(pyridin-3-yl)-1,2,4-oxadiazole | HCID 67026549 | — |
반응 단계
To a solution of 5-(1H-pyrrol-1-yl)nicotinic acid (Maybridge, 188 mg, 1.00 mmol) in dimethylformamide (anhydrous, 5 mL) was added N-(3-methylaminopropyl)-N′-ethylcarbodiimide hydrochloride (EDC) (Aldrich, 192 mg, 1.00 mmol) and 1-hydroxybenzotriazole (HOBT) hydrate (Fluka, 153 mg, 1.00 mmol). The mixture was stirred at ambient temperature for 20 minutes. N′-Hydroxynicotinimidamide (137 mg, 1.0 mmol) was added and the mixture was stirred for 6-10 hours, and then warmed to 140° C. for 2-4 hours. The reaction was cooled to ambient temperature and triturated with water (10 mL). The precipitate was filtered and dried under vacuum to give the titled compound. 1H NMR (300 MHz, DMSO-d6) δ 6.34-6.44 (m, 2H), 7.60-7.82 (m, 3H), 8.50 (dt, J=8.1, 1.9 Hz, 1H), 8.71 (dd, J=2.5, 1.9 Hz, 1H), 8.84 (dd, J=4.6, 1.5 Hz, 1H), 9.21 (d, J=1.7 Hz, 1H), 9.26 (d, J=2.4 Hz, 1H), 9.31 (d, J=1.7 Hz, 1H) ppm; MS (DCI/NH3) m/z 290 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09040568B2 |
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| 출처 데이터셋 | uspto-grants-2015_05 |
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| ORD ID | ord-6d7fc69ff2a445af8695a2ac36a2ad61 |
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| 출처 메모 | uspto-grants-2015_05 |
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