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HRID 2393319作成日:2026年10月25日

Pyridine → HCID 178457339、化合物

https://huagongshe.com/reaction/2393319

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物2-Cyanoethyl tetraisopropylphosphorodiamiditeHCID 128153—
反応物N-[1-[(2R,4S,5R)-4-hydroxy-5-(trityloxymethyl)oxolan-2-yl]-2-oxopyrimidin-4-yl]benzamideHCID 494349—
反応物HCID 178458033HCID 178458033—
溶媒DichloromethaneHCID 6344—
生成物HCID 178457339HCID 17845733962%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05807837
出典データセットuspto-grants-1998_09
ORD IDord-76901d2b60214939b6366170be25f388
出典メモuspto-grants-1998_09