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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1488551생성일: 2026년 10월 27일

Pyridine → HCID 178457339, 화합물

https://huagongshe.com/reaction/1488551

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물2-Cyanoethyl tetraisopropylphosphorodiamiditeHCID 128153—
반응물N-[1-[(2R,4S,5R)-4-hydroxy-5-(trityloxymethyl)oxolan-2-yl]-2-oxopyrimidin-4-yl]benzamideHCID 494349—
반응물HCID 178458033HCID 178458033—
용매DichloromethaneHCID 6344—
생성물HCID 178457339HCID 17845733962%

반응 단계

402 mg (0.7 mmol) of 5'-O-trityl-N-benzoyl-2'-deoxycytidine [prepared as described in step (a) above] were dried by azeotropic distillation with pyridine and then dissolved in 3.5 ml of methylene chloride. 60 mg (0.35 mmol) of diisopropylammonium tetrazolide were added to the solution. 245 μl (0.77 mmol) of 2-cyanoethyl N,N,N',N'-tetraisopropylphosphorodiamidite were then added dropwise, under an atmosphere of argon. The resulting mixture was stirred at room temperature for 3.5 hours under same atmosphere. At the end of this time, the methylene chloride was removed by distillation under reduced pressure. The resulting residue was dissolved in ethyl acetate, and the solution was washed with a 10% w/v aqueous solution of sodium carbonate and with a saturated aqueous solution of sodium chloride, in that order. The solution was then dried over anhydrous magnesium sulfate, after which the solvent was removed by distillation under reduced pressure, and the residue was purified by column chromatography through 23 g of silica gel (70-230 mesh), using ethyl acetate as the eluent, to give 337 mg (yield 62%) of the title compound as a foam substance.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05674856
출처 데이터셋uspto-grants-1997_10
ORD IDord-94af2afc85164d09a65422ce81ed72d3
출처 메모uspto-grants-1997_10