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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33104생성일: 2026년 10월 23일

Cytidine → Benzamide

https://huagongshe.com/ko/reaction/33104

반응식

참여 물질

역할이름HCID투입량
반응물CytidineHCID 6175—
반응물Benzoic anhydrideHCID 7167—
용매DimethylformamideHCID 6228—
생성물BenzamideHCID 2331282.4%

반응 단계

To a suspension of cytidine (100 g, 0.411 mol) in DMF (2.06 L) is added benzoic anhydride (102.4 g, 0.452 mol). The mixture was stirred at room temperature for 20 h. The DMF was removed in vacuo and the residue was triturated with diethyl ether. The resulting solid was collected by suction filtration and washed with diethyl ether (2×200 mL). Further drying in vacuo at room temperature gave the N4 benzamide (140.6 g, 98.3%). A portion of this material (139.3 g, 0.401 mol) was dissolved in anhydrous pyridine (1.2 L) and was treated with 1,3-dichloro-1,1,3,3-tetraisopropyl-disiloxane (141.4 mL, 0.441 mol) at room temp. The solution was stirred at room temperature overnight. The mixture was concentrated to near dryness in vacuo and coevaporated with toluene (3×200 mL). The residue was treated with EtOAc (1.8 L) and washed with HCl (2×200 mL, 0.05 N), NaHCO3 (5%, 2×400 mL). The organic layer was washed dried (Na2SO4), filtered, and evaporated to dryness. Compound 4-1 (256.5 g, >100%) was isolated as a white foam and used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429572B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-584da94920cf4712871774423fd82068
출처 메모uspto-grants-2008_09