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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1051768생성일: 2026년 10월 26일

Thionyl Chloride → 4-Chloro-7H-pyrrolo(2,3-d)pyrimidine-5-carbonitrile

https://huagongshe.com/reaction/1051768

반응식

참여 물질

역할이름HCID투입량
반응물Thionyl ChlorideHCID 24386—
반응물CID 136342890HCID 136342890—
용매DichloromethaneHCID 6344—
생성물4-Chloro-7H-pyrrolo(2,3-d)pyrimidine-5-carbonitrileHCID 22484542—

반응 단계

To a suspension of 4-chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carbaldehyde oxime (G-3) (865 mg, 4.40 mmol, 1.0 eq) in DCM (20 mL), thionyl chloride (3.1 mL, 43.7 mmol, 10.0 eq) is added and the resulting mixture is stirred at RT overnight. The reaction mixture is concentrated in vacuo. The residue is suspended in water (60 mL) and saturated aqueous NaHCO3 is added to adjust the pH to 4. The solid is collected by filtration, rinsed with water and followed by ethyl acetate to afford the first batch of product. The filtrate is extracted with ethyl acetate (3×50 mL). The combined organic layers are washed with brine, dried over Na2SO4 and filtered. The filtrate is concentrated in vacuo and the residue is combined with the above-obtained solid. The product is re-crystallized in ethyl acetate/hexanes (v/v=1/1) and dried in vacuo to afford the product, 4-chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile (G-4).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09388183B2
출처 데이터셋uspto-grants-2016_07
ORD IDord-3bf176cabbf944dead63803e35249963
출처 메모uspto-grants-2016_07