Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19628생성일: 2026년 10월 24일
5-Amino-2-(trifluoromethyl)pyridine → 6-Benzyl-N-(6-(trifluoromethyl)pyridin-3-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amine
https://huagongshe.com/ko/reaction/19628
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 5-Amino-2-(trifluoromethyl)pyridine | HCID 2737744 | — |
| 반응물 | Hydroiodide monohydrate | HCID 21940824 | — |
| 반응물 | 6-Benzyl-4-chloro-5,6,7,8-tetrahydropyrido(4,3-d)pyrimidine | HCID 25324046 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 6-Benzyl-N-(6-(trifluoromethyl)pyridin-3-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amine | HCID 59346545 | 95% |
반응 단계
6-Benzyl-4-chloro-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine (0.5 g, 1.93 mmol) was dissolved in anhydrous dioxane (3 mL) and 6-trifluoromethylpyridin-3-ylamine was added (469 mg, 2.9 mmol), followed by HI/H2O (0.3 mL, 47%). The mixture was heated at 130° C. for 600 s in a Personal Chemistry microwave. The solvents were removed under vacuum and the residue was dissolved in ethyl acetate and washed with sat. NaHCO3 and brine. The organic layer was dried over Na2SO4, filtered and evaporated to give the product as an orange solid (700 mg, 95% crude). The crude product was used for the subsequent step.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07745451B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-65a572b7f1bc4d168ff83ee73c82eb8c |
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| 출처 메모 | uspto-grants-2010_06 |
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