돌아가기
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

반응식

참여 물질

역할이름HCID투입량
반응물5-Amino-2-(trifluoromethyl)pyridineHCID 2737744—
반응물Hydroiodide monohydrateHCID 21940824—
반응물6-Benzyl-4-chloro-5,6,7,8-tetrahydropyrido(4,3-d)pyrimidineHCID 25324046—
용매1,4-DioxaneHCID 31275—
생성물6-Benzyl-N-(6-(trifluoromethyl)pyridin-3-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amineHCID 5934654595%

반응 조건

온도130 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745451B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-65a572b7f1bc4d168ff83ee73c82eb8c
출처 메모uspto-grants-2010_06