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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 341440생성일: 2026년 10월 26일

1,4-Diazabicyclo(2.2.2)octane--trimethylalumane (1/2) → 2-N-Methyl-2-N-phenyl-6-(5-{5H,6H,7H-pyrrolo[3,4-d]pyrimidin-6-yl}-1,2,4-oxadiazol-3-yl)-1,3,5-triazine-2,4-diamine

https://huagongshe.com/reaction/341440

반응식

참여 물질

역할이름HCID투입량
반응물1,4-Diazabicyclo(2.2.2)octane--trimethylalumane (1/2)HCID 16688366—
반응물6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidine hydrochlorideHCID 54758847—
반응물N-methyl-N-phenyl-6-(5-trichloromethyl-[1,2,4]oxadiazol-3-yl)-[1,3,5]triazine-2,4-diamineHCID 66802564—
용매TetrahydrofuranHCID 8028—
생성물2-N-Methyl-2-N-phenyl-6-(5-{5H,6H,7H-pyrrolo[3,4-d]pyrimidin-6-yl}-1,2,4-oxadiazol-3-yl)-1,3,5-triazine-2,4-diamineHCID 569419818.3%

반응 단계

To a solution of 6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidine hydrochloride salt (38 mg, 0.231 mmol) in anhydrous THF (3 mL) was added DABAL-Me3 (bis(trimethylaluminum)-1,4-diazabicyclo[2.2.2]-octane) (57 mg, 0.231 mmol) at room temperature. The solution was heated under nitrogen at 40 C for 3 h and N-methyl-N-phenyl-6-(5-trichloromethyl-[1,2,4]oxadiazol-3-yl)-[1,3,5]triazine-2,4-diamine (Intermediate 60, 60 mg, 0.155 mmol) was added. The resulting reaction mixture was heated at 80 C for 5 h and then quenched with water (2 mL) drop-wise. The solution was extracted into EtOAc (3×25 mL) and the combined organics washed with a 1M aq. solution of HCl (20 mL), brine (20 mL), dried over magnesium sulfate, evaporated to dryness and purified by preparative HPLC-MS (Method B) to afford the title compound as a white solid (5 mg, 8%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895733B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-a8746bf53f9b45dbaec911bf523476bf
출처 메모uspto-grants-2014_11