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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19636생성일: 2026년 10월 23일

Triethylamine → 5,6,7,8-Tetrahydro-N-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-6-m-tolylpyrido[4,3-d]pyrimidin-4-amine

https://huagongshe.com/ko/reaction/19636

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-Tolylboronic acidHCID 2733950—
반응물5,6,7,8-Tetrahydro-N-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)pyrido[4,3-d]pyrimidin-4-amineHCID 59346495—
촉매Cupric acetateHCID 8895—
용매TetrahydrofuranHCID 8028—
생성물5,6,7,8-Tetrahydro-N-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-6-m-tolylpyrido[4,3-d]pyrimidin-4-amineHCID 684131289.6%

반응 단계

5,6,7,8-Tetrahydro-N-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)pyrido[4,3-d]pyrimidin-4-amine (110 mg, 0.39 mmol) was dissolved in anhydrous THF (2 mL). To the mixture was added m-tolylboronic acid (105 mg, 0.78 mmol), Cu(OAc)2 (141 mg, 0.78 mmol) and triethylamine (0.68 g, 0.095 mL) and 390 mg of crushed, activated 4 A molecular seives. The mixture was agitated for 6 h and the solvent was removed under vacuum. The residue was purified using a gradient of ethyl acetate:hexane (0-100%) to give the desired compound as reddish powder (14 mg, 9.6%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745451B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-96d11f32c81e46d482f0855c913c1994
출처 메모uspto-grants-2010_06