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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 417880생성일: 2026년 10월 24일

Hydrogen Peroxide → 4-(2-amino-4-chloro-7-((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl)but-3-ynyl di-tert-butyl phosphate

https://huagongshe.com/ko/reaction/417880

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물Sodium BicarbonateHCID 516892—
반응물Di-tert-butyl N,N-DiisopropylphosphoramiditeHCID 853005—
반응물4-[2-Amino-4-chloro-7-(4-methoxy-3,5-dimethyl-pyridin-2-ylmethyl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl]-but-3-yn-1-olHCID 11950510—
반응물HCID 178418441HCID 178418441—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물4-(2-amino-4-chloro-7-((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl)but-3-ynyl di-tert-butyl phosphateHCID 57713854—

반응 조건

온도0 °C

반응 단계

A solution of 4-[2-Amino-4-chloro-7-(4-methoxy-3,5-dimethyl-pyridin-2-ylmethyl)-7H-pyrrolo [2,3-d]pyrimidin-5-yl]-but-3-yn-1-ol (see example 2) (4.0 g) and 1-H-tetrazole (0.45 M in acetonitrile, 70 mL) in THF (160 mL) was treated with di-tert-butyl diisopropylphosphoramidite (16.4 mL) at rt for 2 h. The solution was cooled to 0° C. and treated with 30% aqueous H2O2 (11 mL) for 30 min. Work-up (EtOAc, aq. NaHCO3) and reverse-phase preparative HPLC gave the title compound, as a solid. HPLC Rt=6.13 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093229B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-4c744ce333734f9187fff09fd72a4ccf
출처 메모uspto-grants-2012_01