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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1945638생성일: 2026년 10월 25일

Acetic Acid → 2-{1-[2-(2-Chloro-9-methyl-6-morpholin-4-yl-9H-purin-8-yl)ethyl]piperidin-4-yl}propan-2-ol

https://huagongshe.com/reaction/1945638

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Trimethyl orthoformateHCID 9005—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물2-(4-Piperidyl)-2-propanolHCID 5200321—
반응물(2-chloro-9-methyl-6-morpholin-4-yl-9H-purin-8-yl)acetaldehydeHCID 59605819—
용매1,2-DichloroethaneHCID 11—
생성물2-{1-[2-(2-Chloro-9-methyl-6-morpholin-4-yl-9H-purin-8-yl)ethyl]piperidin-4-yl}propan-2-olHCID 59605738—

반응 단계

To a solution of (2-chloro-9-methyl-6-morpholin-4-yl-9H-purin-8-yl)acetaldehyde (150 mg, 0.51 mmol) in DCE (10 mL) was added 2-piperidin-4-ylpropan-2-ol (110 mg, 0.77 mmol), trimethyl orthoformate (0.55 mL, 5.02 mmol) and acetic acid (0.03 mL, 0.52 mmol). The reaction mixture was stirred at room temperature for 5 h, sodium triacetoxyborohydride (154 mg, 0.73 mmol) was added and the resulting mixture stirred for a further 2 h. The reaction mixture was loaded onto an Isolute® SCX-2 cartridge, the cartridge was washed with MeOH then the desired product eluted with 2 M NH3 in MeOH. The resulting residue was purified by column chromatography (Si—PCC, 0-10% MeOH in DCM) to give the title compound as an off white solid (109 mg, 51%). LCMS (Method H): RT=2.54 min, [M+H]+ 423.5

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08394796B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-2009ad6871b94ef7b4dc237adfb212ee
출처 메모uspto-grants-2013_03