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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1066425생성일: 2026년 10월 27일

Chloride → N4-Benzoyl-2'-O-propylcytidine

https://huagongshe.com/reaction/1066425

반응식

참여 물질

역할이름HCID투입량
반응물ChlorideHCID 312—
반응물Benzoyl chlorideHCID 7412—
반응물Ammonium HydroxideHCID 14923—
반응물2'-O-PropylcytidineHCID 22874746—
용매WaterHCID 962—
용매PyridineHCID 1049—
생성물N4-Benzoyl-2'-O-propylcytidineHCID 22874774—

반응 단계

To the 2′-O-propylcytidine reaction mixture of Example 82 in an ice bath was added pyridine (60 ml) and trimethylsilIyl chloride (60 ml). The reaction was stirred for 30 mins followed by the addition of benzoyl chloride (55 ml). The resulting reaction mixture was stirred for 2.5 hr. and then cooled in an ice bath. H2O (100 ml) and conc. NH4OH (100 ml) were added. After stirring for 30 mins, the reaction mixture was evaporated and the residue partition between H2O and CH2Cl2. The organic phase was washed once with dil Na2CO3, once with dil HCl, dried over MgSO4 and evaporated. The resulting residue was loaded on a silica gel column (150 g) and eluted with first CH2Cl2 then 5 to 10% MeOH in CH2Cl2 as the elution solvent. The product containing fractions were evaporated to a foam. The foam was crystallized from EtOAc/Hexanes to give the product (6.5 g total) in several crystal batches.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06242592B1
출처 데이터셋uspto-grants-2001_06
ORD IDord-a5f7d5bee44e4691853602d77dd5d71d
출처 메모uspto-grants-2001_06