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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 478191생성일: 2026년 10월 24일

Dimethylformamide dimethyl acetal → 5-[2-(3-Nitrophenylamino)-5-methyl-pyrimidin-4-yl]-4-cyclohexyl-2-methylsulfanyl-thiophene-3-carbonitrile

https://huagongshe.com/ko/reaction/478191

반응식

참여 물질

역할이름HCID투입량
반응물Dimethylformamide dimethyl acetalHCID 78373—
반응물4-Cyclohexyl-5-(3-dimethylamino-2-methyl-acryloyl)-2-methylsulfanyl-thiophene-3-carbonitrileHCID 69555274—
반응물HCID 178418758HCID 178418758—
용매TolueneHCID 1140—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물5-[2-(3-Nitrophenylamino)-5-methyl-pyrimidin-4-yl]-4-cyclohexyl-2-methylsulfanyl-thiophene-3-carbonitrileHCID 2201902842%

반응 조건

온도90 °C

반응 단계

To a solution of 4-cyclohexyl-5-(3-dimethylamino-2-methyl-acryloyl)-2-methylsulfanyl-thiophene-3-carbonitrile (0.5 g, 1.7 mmol) in toluene (3 ml) was added DMF-DMA and the reaction was heated at 90° C. overnight resulting in conversion to product as determined by TLC (40% EtOAc:hexanes). The crude product was combined with DMF (10 ml) and 3-Nitrophenylguanidine (0.5 g, 2.78 mmol) in a sealed tube and heated at 120° C. overnight resulting in conversion to product as determined by TLC (40% EtOAc:hexanes). The reaction was partitioned between EtOAc and water, the organics were dried over sodium sulfate then concentrated in vacuo. The crude product was purified by chromatography (silica gel, 10% EtOAC:hexanes) to afford 0.334 g (3.05 umol) of V-7 in 42% yield for 2 steps. 1H NMR (CDCl3) δ1.0-2.0 (m, 10H), 2.1 (s, 3H), 2.6(s, 3H), 7.4(m, 1H), 7.7 (d, 1H), 7.8 (d, 1H), 8.3 (s, 1H), 8.7 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06642227B2
출처 데이터셋uspto-grants-2003_11
ORD IDord-6b13f0f56ddc4635806ba795084de9b6
출처 메모uspto-grants-2003_11