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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2-Chloro-5-nitropyrimidin-4-yl thiocyanate | HCID 21077588 | — |
| 반응물 | 3-Amino-4-{[(2,4-dimethoxyphenyl)methyl]amino}benzonitrile | HCID 56605243 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 2-(5-Cyano-2-{[(2,4-dimethoxyphenyl)methyl]amino}anilino)-5-nitropyrimidin-4-yl thiocyanate | HCID 56605211 | 6.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07884109B2 |
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| 출처 데이터셋 | uspto-grants-2011_02 |
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| ORD ID | ord-c869e2adaff745a893465ba7ca8a81b5 |
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| 출처 메모 | uspto-grants-2011_02 |
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