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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 448666생성일: 2026년 10월 23일

Hexamethyldisilazane → 3'-Deoxy-5'-O-(4-methoxytrityl)-3'-methyl-2'-O-(2-methoxyethyl)-5-methyluridine

https://huagongshe.com/ko/reaction/448666

반응식

참여 물질

역할이름HCID투입량
반응물HexamethyldisilazaneHCID 13838—
반응물DiisopropylethylamineHCID 81531—
반응물3'-Deoxy-5'-O-(4-methoxytrityl)-3'-(iodomethyl)-2'-O-(2-methoxyethyl)-5-methyluridineHCID 23518332—
반응물HCID 178418291HCID 178418291—
용매DichloromethaneHCID 6344—
용매THF MeOH NEt3HCID 67203757—
생성물3'-Deoxy-5'-O-(4-methoxytrityl)-3'-methyl-2'-O-(2-methoxyethyl)-5-methyluridineHCID 2351833358.9%

반응 조건

온도105 °C

반응 단계

A mixture of ammonium phosphinate (410 mg, 5.1 mmol) and 1,1,1,3,3,3-hexamethyldisilazane (1.18 mL, 0.90 g, 5.59 mmol) was heated at 100-110° C. for 2 h under nitrogen atmosphere with condenser. The intermediate BTSP(bis[trimethylsilyl]phosphinate) was cooled to 0° C. and 5 mL of dichloromethane was injected. To this mixture was injected a solution of 3′-deoxy-5′-O-(4-methoxytrityl)-3′-(iodomethyl)-2′-O-(2-methoxyethyl)-5-methyluridine (0.78 g, 1.1 mmol) and diisopropylethylamine (0.39 mL, 287 mg, 2.23 mmol) in 7 mL of dichloromethane. After the reaction mixture was stirred at rt overnight, a mixture of THF-MeOH-NEt3 (3/6/0.3 mL) was added and continued to stir for 1 h. The reaction mixture was filtered through a pad of celite and washed with dichloromethane. The solvent was evaporated and the residue was purified by flash chromatography on a silica gel column using 2:1, 1:1, and then 1:2 hexanes-EtOAc as eluent providing 380 mg of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481712B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-e71e1b50414041fca18a48d67dea5682
출처 메모uspto-grants-2013_07