돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38105생성일: 2026년 10월 25일

Dibromomethane → 1-(3-Dibenzylamino-2,6-difluoro-phenyl)-2-[1,3]dithietan-2-ylidene-2-pyridin-4-yl-ethanone

https://huagongshe.com/reaction/38105

반응식

참여 물질

역할이름HCID투입량
반응물DibromomethaneHCID 3024—
반응물Carbon DisulfideHCID 6348—
반응물Potassium CarbonateHCID 11430—
반응물1-(3-Dibenzylamino-2,6-difluoro-phenyl)-2-pyridin-4-yl-ethanoneHCID 58477120—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물1-(3-Dibenzylamino-2,6-difluoro-phenyl)-2-[1,3]dithietan-2-ylidene-2-pyridin-4-yl-ethanoneHCID 5847709349%

반응 단계

To a solution of 1-(3-Dibenzylamino-2,6-difluoro-phenyl)-2-pyridin-4-yl-ethanone (2.14 g, 4.994 mmol) in dry DMSO (22 mL) under nitrogen atmosphere solid potassium carbonate (2.07 g, 15 mmol, 3 eq) was added at room temperature, followed by carbon disulfide (0.9 mL, 15 mmol, 3 eq) and dibromomethane (1.05 mL, 15 mmol, 3 eq). The reaction mixture was stirred at room temperature for 3 hour and then poured into stirred iced water (150 mL). The aqueous phase was extracted with ethyl acetate (3 x 70 mL) and the combined organic layers were washed with water, dried and concentrated under reduced pressure. The crude product was purified by silica gel chromatography (n-hexane/ethyl acetate 7:3 to 6:4) to obtain 1.26 g of 1-(3-dibenzylamino-2,6-difluoro-phenyl)-2-[1,3]dithietan-2-ylidene-2-pyridin-4-yl-ethanone as yellow solid (49%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524707B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-17697ae026424e0b9282ea5373648abf
출처 메모uspto-grants-2013_09