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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 538924생성일: 2026년 10월 27일

Cesium carbonate → (3aR,6aR)-3-(6-Chloro-2-morpholinopyrimidin-4-yl)tetrahydrofuro[3,4-d]oxazol-2(3H)-one

https://huagongshe.com/reaction/538924

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참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물Sodium BicarbonateHCID 516892—
반응물4-(4,6-Dichloropyrimidin-2-yl)morpholineHCID 2772068—
반응물(3aR,6aR)-tetrahydrofuro[3,4-d]oxazol-2(3H)-oneHCID 55303430—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
촉매Argon 4,5-bis(diphenylphosphino)-9,9-dimethylxantheneHCID 86694355—
용매1,4-DioxaneHCID 31275—
생성물(3aR,6aR)-3-(6-Chloro-2-morpholinopyrimidin-4-yl)tetrahydrofuro[3,4-d]oxazol-2(3H)-oneHCID 8669435488.6%

반응 조건

온도85 °C

반응 단계

To a solution of (3aR,6aR)-tetrahydrofuro[3,4-d]oxazol-2(3H)-one (500 mg, 3.87 mmol), 4-(4,6-dichloropyrimidin-2-yl)morpholine (1088 mg, 4.65 mmol) and Cs2CO3 (2.14 g, 6.58 mmol) in dioxane (20 mL) was added after degassing with argon 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (157 mg, 0.271 mmol) and Pd2(dba)3 (70.9 mg, 0.077 mmol) and the reaction mixture was heated for 6 h at 85° C. The reaction mixture was added to 10% aqueous NaHCO3 solution and extracted with EtOAc. Combined extracts were washed with brine, dried over MgSO4, filtered and concentrated. The crude product was triturated in MeOH overnight, filtered off and dried to afford the title compound as a colorless solid (1.12 g, 87%): tR=0.92 min (LC-MS 3); ESI-MS: 327, 329 [M+H]+ (LC-MS 3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08865894B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-bda22b43dbb34821baabd86acef054a1
출처 메모uspto-grants-2014_10