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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2362820생성일: 2026년 10월 26일

1,3-Dichloroacetone → 2-Amino-4-[4-(2-azidoethoxy)phenyl]-6-[({2-[(4-fluorophenyl)amino]-1,3-thiazol-4-yl}methyl)thio]pyridine-3,5-dicarbonitrile

https://huagongshe.com/reaction/2362820

반응식

참여 물질

역할이름HCID투입량
반응물1,3-DichloroacetoneHCID 10793—
반응물Sodium BicarbonateHCID 516892—
반응물4-FluorophenylthioureaHCID 693061—
반응물HCID 178510482HCID 178510482—
용매EthanolHCID 702—
생성물2-Amino-4-[4-(2-azidoethoxy)phenyl]-6-[({2-[(4-fluorophenyl)amino]-1,3-thiazol-4-yl}methyl)thio]pyridine-3,5-dicarbonitrileHCID 86624336—

반응 단계

A solution of 74 mg (0.44 mmol) of 4-fluorophenylthiourea and 55 mg (0.44 mmol) of 1,3-dichloroacetone in 5 ml of ethanol is stirred at +85° C. for 60 min. After removal of the solvent on a rotary evaporator, the residue is taken up in 5 ml of DMF, 105 mg (0.31 mmol) of the compound from Example 38A and 78 mg (0.93 mmol) of sodium bicarbonate are added and the mixture is then stirred at RT for 20 h. The mixture is then added to 15 ml of saturated sodium bicarbonate solution. The mixture is extracted with ethyl acetate (three times, 15 ml each) and the combined organic phases are dried over magnesium sulphate. After removal of the solvent on a rotary evaporator, the crude product is purified chromatographically on silica gel 60 (mobile phase gradient dichloromethane/ethanol 200:1→20:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08691850B2
출처 데이터셋uspto-grants-2014_04
ORD IDord-d1b5202be6064da1a2e0e2712e3d42ab
출처 메모uspto-grants-2014_04