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HRID 869482作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/869482

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物CID 136342890HCID 136342890—
溶媒DichloromethaneHCID 6344—
生成物4-Chloro-7H-pyrrolo(2,3-d)pyrimidine-5-carbonitrileHCID 2248454297.1%

反応手順

To a suspension of 4-chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carbaldehyde oxime (865 mg, 4.40 mmol, 1.0 eq) in DCM (20 mL), thionyl chloride (3.1 mL, 43.7 mmol, 10.0 eq) was added and the resulting mixture was stirred at RT overnight. The reaction mixture was concentrated in vacuo. The residue was suspended in water (60 mL) and saturated aqueous NaHCO3 was added to adjust the pH to 4. The solid was collected by filtration, rinsed with water followed by ethyl acetate to afford the first batch of product. The filtrate was then extracted with ethyl acetate (50 mL×3). The combined organic layer was washed with brine, dried over Na2SO4 and filtered. The filtrate was concentrated in vacuo and the residue was combined with the above-obtained solid. The crude product was then re-crystallized in ethyl acetate/hexanes (1:1) and dried in vacuo to afford 4-chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile (763 mg, 97% yield). ESI-MS m/z: 178.8 [M+H]+, 176.8 [M−H]−.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08969363B2
出典データセットuspto-grants-2015_03
ORD IDord-189c78c7fe614f1ba5dc618b0182e9f5
出典メモuspto-grants-2015_03