Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 277055생성일: 2026년 10월 26일
p-Toluenesulfonic acid → Diethyl-(2-phenyl-7-pyridin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-5-yl)-amine
https://huagongshe.com/reaction/277055
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | Ethyl p-methylbenzenesulfonate | HCID 6638 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 2-Phenyl-7-pyridin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-5-ylamine | HCID 22629700 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Diethyl-(2-phenyl-7-pyridin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-5-yl)-amine | HCID 9906109 | 15% |
반응 단계
A solution of 0.29 g (0.001 mol) 2-phenyl-7-pyridin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-5-ylamine in 50 ml dimethylformamide was treated with 0.05 g (0.001 mol) sodiumhydride(55%) for 15 minutes at room temperature. Then 0.22 g (0.001 mol) ethyl-p-toluenesulfonate were added and stirring was continued for 22 hours. Addition of sodiumhydride and p-toluenesulfonate was repeated three times. After each addition stirring was continued at 50° C. for 20 hours. Saturated aqueous sodiumbicarbonate was added and the mixture was extracted with dichloromethane. Evaporation of the solvent and chromatography on silicagel with dichloromethane/methanol 96/4 gave 0.05 g (15%) diethyl-(2-phenyl-7-pyridin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-5-yl)-amine as yellow oil. MS m/e (%): 343 (M+, 59), 314 (100), 300 (73), 104 (51).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06355653B1 |
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| 출처 데이터셋 | uspto-grants-2002_03 |
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| ORD ID | ord-38f8a5076cc64aeeac9ae0163886b886 |
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| 출처 메모 | uspto-grants-2002_03 |
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