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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 390940생성일: 2026년 10월 23일

Trimethyl orthoformate → 2-Chloro-6-((4-(methylsulfonyl)piperazin-1-yl)methyl)-4-morpholinofuro[3,2-d]pyrimidine

https://huagongshe.com/ko/reaction/390940

반응식

참여 물질

역할이름HCID투입량
반응물Trimethyl orthoformateHCID 9005—
반응물Sodium AcetateHCID 517045—
반응물1-(Methylsulfonyl)piperazineHCID 709161—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물2-Chloro-4-morpholinofuro[3,2-d]pyrimidine-6-carbaldehydeHCID 56833742—
용매1,2-DichloroethaneHCID 11—
생성물2-Chloro-6-((4-(methylsulfonyl)piperazin-1-yl)methyl)-4-morpholinofuro[3,2-d]pyrimidineHCID 5683374468%

반응 단계

2-Chloro-4-morpholinofuro[3,2-d]pyrimidine-6-carbaldehyde 39 prepared following Example 20 (65 mg, 1.0 eq) was dissolved in 1,2-dichloroethane (9.7 ml) and treated with hydrochloride salt of 1-methanesulfonylpiperazine (69 mg, 1.4 eq), sodium acetate (28 mg, 1.4 eq) and trimethyl orthoformate (0.27 ml, 10 eq). Reaction mixture was stirred at r.t. for 12 h. Sodium triacetoxyborohydride (62 mg, 1.2 eq) was added and reaction mixture was stirred at r.t. for 8 h. Reaction mixture was quenched with saturated aq. NaHCO3 and extracted with dichloromethane. The combined organic layers were dried (Na2SO4) and concentrated. The crude reaction mixture was purified by flash chromatography to yield 2-chloro-6-((4-(methylsulfonyl)piperazin-1-yl)methyl)-4-morpholinofuro[3,2-d]pyrimidine (70 mg, 68%): MS (Q1) 416 (M)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383620B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-ccbfd02770054dbfb22ee0f1831f6b9e
출처 메모uspto-grants-2013_02