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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1051766생성일: 2026년 10월 27일

Dimethylformamide → 4-Chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carbaldehyde

https://huagongshe.com/reaction/1051766

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidineHCID 5380710—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물4-Chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carbaldehydeHCID 56763828—

반응 조건

온도-78 °C

반응 단계

To a solution of 5-bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine (G-1) (2.33 g, 10.0 mmol, 1.0 eq) in anhydrous THF (100 mL) at −78° C. under argon, n-BuLi solution (2.5 M in THF, 8.8 mL, 22.0 mmol, 2.2 eq) is added dropwise (over 10 min). The resulting mixture is stirred at −78° C. for 1 h and then DMF (2.0 g, 11.0 mmol, 1.1 eq) is added dropwise (over 10 min). The mixture is stirred at −78° C. for an additional 30 min and then stirred at RT overnight. The reaction mixture is quenched with H2O (50 mL) and then concentrated in vacuo. The residue is triturated with saturated aqueous NH4Cl solution. The solid is collected by filtration, rinsed with ethyl acetate, and dried in vacuo to afford the product, 4-chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carbaldehyde (G-2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09388183B2
출처 데이터셋uspto-grants-2016_07
ORD IDord-586035db7d394c5eb496f97f23d4e171
출처 메모uspto-grants-2016_07