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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51496생성일: 2026년 10월 24일

Sodium hydride → 2-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]-butyrolactone

https://huagongshe.com/ko/reaction/51496

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참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2(3H)-Furanone, 3-bromodihydro-HCID 95463—
반응물5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-ylamineHCID 12042234—
용매DimethylformamideHCID 6228—
생성물2-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]-butyrolactoneHCID 22736241—

반응 조건

온도0 °C

반응 단계

4-Amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidine (1.0 g) was added to a mixture of sodium hydride (0.158 g of a 60% dispersion in mineral oil) in dimethyl formamide (70 ml) with stirring under nitrogen at 0° C. The mixture was stirred at 0° C. for 1 hour and then α-bromo-γ-butyrolactone (0.60 g) in dimethylformamide (6 ml) was added dropwise with stirring at 0° C. The mixture was stirred at ambient temperature for 18 hours and then quenched with water (100 ml). The mixture was extracted with ethyl acetate. The combined extracts were dried and evaporated to give 2-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]-butyrolactone as an oil which was used directly in b).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713474B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-6f66962956a94b1cb544567f732d7e9e
출처 메모uspto-grants-2004_03