돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 889589생성일: 2026년 10월 25일

Tetrahydrofuran → 2-trimethylsilanyl-ethoxymethyl-7H-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/889589

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Sodium hydrideHCID 24758—
반응물7H-Pyrrolo(2,3-d)pyrimidineHCID 261591—
반응물2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
생성물2-trimethylsilanyl-ethoxymethyl-7H-pyrrolo[2,3-d]pyrimidineHCID 86617481—

반응 단계

7H-Pyrrolo[2,3-d]pyrimidine (1.16 g, 9.74 mmol), was dissolved in 100 ml anhydrous THF under N2. At 0° C., a 60% dispersion of NaH 0.51 g in mineral oil was added. The mixture was stirred at ambient temperature and 2.93 ml (9.8 mmol) (2-chloromethoxy-ethyl)-trimethyl-silane dissolved in 15 ml anhydrous THF was added. The reaction mixture was stirred at room temperature for 2 hour and subsequently concentrated in vacuo. Ethyl acetate was added to the mixture and the organic layer was washed three times with a saturated NaHCO3 solution, dried (Na2SO4), filtered and concentrated. The resulting residue was purified by flash chromatography (diethyl ether) to afford 7-(2-trimethylsilanyl-ethoxymethyl-7H-pyrrolo[2,3-d]pyrimidine (compound 91), (amorphous, 0.84 g, 35%). 1H-NMR (400 MHz, CDCl3): δ 9.1 (bs, 1H), 9.0 (bs, 1H), 7.43 (bd, J=4 Hz, 1H), 6.68 (bd, J=4 Hz, 1H), 5.73 (s, 1H), 3.6 (t, J=8 Hz, 2H), 0.97 (t, J=8 Hz, 2H), 0.1 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08252930B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-4c1ad12326724c35bd87d949d9632358
출처 메모uspto-grants-2012_08