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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 844537생성일: 2026년 10월 24일

Chlorotrimethylsilane → Deoxycytidine

https://huagongshe.com/ko/reaction/844537

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물Thionyl ChlorideHCID 24386—
반응물Deoxycytidine hydrochlorideHCID 107488—
반응물Ethanol, 2-methoxy-, benzoateHCID 85839854—
반응물Benzoyl chloride;2-methoxyethanolHCID 131723206—
용매PyridineHCID 1049—
생성물DeoxycytidineHCID 1371182.4%

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온도0 °C

반응 단계

2′-deoxycytidine monohydrochloride (13.18 g, 52 mmol) that had been subjected to azeotropic dehydration with pyridine (2×20 ml) under an argon gas stream was suspended in anhydrous pyridine (120 ml) and cooled to 0° C. Chlorotrimethylsilane (19.0 ml, 150 mmol) was added and the mixture was stirred for 15 minutes. The benzoyl chloride-monomethoxypolyethylene glycol; CH3O(CH2CH2O)kC6H4COCl {34.9 mmol, mPEG portion Mn=350; 1H-NMR (400 MHz, CDCl3, TMS) δ68.07 (d, J=8.8Hz,2H,ArH), 6.99 (d, J=8.8 Hz,2H,ArH), 4.23 (t, J=4.8 Hz,2H,ArOCH2), 3.89 (t, J=4.8 Hz,2H,OCH2), 3.79-3.51 (m), 3.38(s,3H,OCH3) ppm} prepared by the reaction of benzoic acid-monomethoxypolyethylene glycol (C. J. van Staveren, et al., J. Am. Chem. Soc., 110, 4994 (1988)) with thionyl chloride, was dissolved in anhydrous pyridine (80 ml) under an argon gas stream, and was added to the previously prepared reaction solution and stirred at room temperature for 2 hours. After cooling to 0° C., distilled water ((10 ml) was added to the reaction mixture , and after concentration to approximately 1/2, concentrated ammonium hydroxide (20 ml) was added at 0° C. and the mixture was stirred for 20 minutes. The solvent was removed under reduced pressure, a saturated sodium bicarbonate aqueous solution (200 ml) was added, and extraction was performed with chloroform (3×100 ml). The organic layer was washed with water a (2×200 ml) and dried over anhydrous sodium sulfate. After filtration, the filtrate was condensed under reduced pressure and the residue was purified by silica gel column chromatography (chloroform/methanol=100/5) to obtain the target PEG-modified 2′-deoxycytidine represented by the formula (3′-1) (18.85 g, 82.4% yield). The 1H-NMR of the obtained compound (400 MHz, CDCl3, TMS) was δ=9.30 (brs,1H,NH), 8.41 (d, J=7.2 Hz,1H,H6), 7.83 (d, J=7.6 Hz,2H,ArH), 7.48 (br,1H,H5), 6.92 (d, J=7.6 Hz,2H,ArH), 6.29-6.10 (m,1H,H1′), 5.07 (brs,1H), 4.74-4.40 (br,2H), 4.27-4.00 (m,3H), 4.00-3.42 (m), 3.36 (s,3H,OCH3), 2.70-2.50 (m,1H,H2″), 2.35-2.18 (m,1H,H2′) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06380378B1
출처 데이터셋uspto-grants-2002_04
ORD IDord-e4a7d50e4eea41f1acf68351e0ec1ac7
출처 메모uspto-grants-2002_04