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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hexamethyldisilazane | HCID 13838 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 3'-Deoxy-5'-O-(4-methoxytrityl)-3'-(iodomethyl)-2'-O-(2-methoxyethyl)-5-methyluridine | HCID 23518332 | — |
| 반응물 | HCID 178418291 | HCID 178418291 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | THF MeOH NEt3 | HCID 67203757 | — |
| 생성물 | 3'-Deoxy-5'-O-(4-methoxytrityl)-3'-methyl-2'-O-(2-methoxyethyl)-5-methyluridine | HCID 23518333 | 58.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08481712B2 |
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| 출처 데이터셋 | uspto-grants-2013_07 |
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| ORD ID | ord-e71e1b50414041fca18a48d67dea5682 |
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| 출처 메모 | uspto-grants-2013_07 |
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