참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzonitrile | HCID 7505 | — |
| 반응물 | 1,10-Phenanthroline hydrate | HCID 21226 | — |
| 반응물 | 2,4-Diaminopyridine | HCID 68036 | — |
| 촉매 | copper(I) bromide | HCID 24593 | — |
| 생성물 | 2-Phenyl-[1,2,4]triazolo[1,5-a]pyridin-7-ylamine | HCID 67774145 | 29% |
반응 단계
A mixture of 2,4-diamino-pyridine (1.26 g, 11.5 mmol), copper (I) bromide (82.8 mg, 0.57 mmol), 1,10-phenanthroline monohydrate (114.0 mg, 0.57 mmol) and benzonitrile (13 mL) was heated in a 50 mL 3-necked flask to 150° C. During 41 h a gentle flow of O2/N2 (5:95) was bubbled through the reaction mixture (conversion 42%, HPLC method see below). The reaction mixture was then filtered. The resulting clear brown solution was evaporated to dryness and the crude was product purified by silica gel chromatography (hexane/EtOAc 2:8) to yield 7-amino-2-phenyl-[1,2,4]triazolo[1,5-a]pyridine (0.72 g, 29%) as a light yellow solid with 99.0% purity (HPLC area-%, HPLC method: X-Bridge C18 column, 150×4.6 mm; mobile phase, A: water/NCMe (95:5), B: NCMe, C: NBu4HSO4 buffer pH 3-4; flow: 1.5 ml/min; gradient from 90/0/10 (A/B/C) to 5/85/10 (A/B/C) within 6 min, isocratic 5/85/10 (A/B/C) for 4 min. Retention time: 0.95 min (2,4-diamino-pyridine), 4.08 min (7-amino-2-phenyl-[1,2,4]triazolo[1,5-a]pyridine)).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09115130B2 |
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| 출처 데이터셋 | uspto-grants-2015_08 |
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| ORD ID | ord-065e9c5424fd4c06b95d96d4f455d4a3 |
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| 출처 메모 | uspto-grants-2015_08 |
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