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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1363242생성일: 2026년 10월 27일

Potassium Carbonate → 2-(5-Cyano-2-{[(2,4-dimethoxyphenyl)methyl]amino}anilino)-5-nitropyrimidin-4-yl thiocyanate

https://huagongshe.com/reaction/1363242

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참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2-Chloro-5-nitropyrimidin-4-yl thiocyanateHCID 21077588—
반응물3-Amino-4-{[(2,4-dimethoxyphenyl)methyl]amino}benzonitrileHCID 56605243—
용매AcetonitrileHCID 6342—
생성물2-(5-Cyano-2-{[(2,4-dimethoxyphenyl)methyl]amino}anilino)-5-nitropyrimidin-4-yl thiocyanateHCID 566052116.5%

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온도0 °C

반응 단계

A solution of 4-(2,4-dimethoxybenzylamino)-3-aminobenzonitrile (3.9 g) in acetonitrile (100 mL) was cooled to 0° C. and treated with potassium carbonate (6.3 g) followed by a solution containing 3 g of 2-chloro-5-nitro-4-thiocyanatopyrimidine (WO 2003/032994) in acetonitrile (50 mL). The mixture was stirred for 30 minutes at 0° C. and 30 minutes at room temperature resulting in the formation of a precipitate. The mixture was quenched at 0° C. by the addition of 4% acetic acid (150 mL) and filtered. The precipitate was swirled in 100 mL acetonitrile and filtered again. The precipitate was washed with acetonitrile, which resulted in the slow dissolution of product into the filtrate. After air-drying, 1.5 g of the title compound remained as the precipitate cake. The filtrate was extracted with EtOAc, dried over Na2SO4, filtered, and concentrated in vacuo. Column chromatography (0→20% EtOAc/DCM) and recrystallization from acetonitrile provided 0.415 g of additional title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07884109B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-c869e2adaff745a893465ba7ca8a81b5
출처 메모uspto-grants-2011_02