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HRID 1094785생성일: 2026년 10월 26일

Heptane → N-[6-Amino-5-(2,5-dichloro-3-methoxyphenyl)pyridin-2-yl]-4-methyl-1,2,5-oxadiazole-3-carboxamide

https://huagongshe.com/reaction/1094785

반응식

참여 물질

역할이름HCID투입량
반응물HeptaneHCID 8900—
반응물Oxalyl chlorideHCID 65578—
반응물4-Methyl-1,2,5-oxadiazole-3-carboxylic acidHCID 314768—
반응물3-(2,5-Dichloro-3-methoxyphenyl)-pyridine-2,6-diamineHCID 66637041—
촉매DimethylformamideHCID 6228—
용매PyridineHCID 1049—
용매AcetonitrileHCID 6342—
용매Thionyl ChlorideHCID 24386—
생성물N-[6-Amino-5-(2,5-dichloro-3-methoxyphenyl)pyridin-2-yl]-4-methyl-1,2,5-oxadiazole-3-carboxamideHCID 2515596118%

반응 조건

온도50 °C

반응 단계

4-Methyl-1,2,5-oxadiazole-3-carboxylic acid (0.3 g, 2.34 mmol) was stirred in thionyl chloride (10 ml) at 50° C. for 18 hours. A further 3 ml oxalyl chloride and 2 drops of dimethylformamide were added and the reaction stirred for a further 1.5 hours at 50° C. The reaction was concentrated in vacuo and azeotroped with dichloromethane. The residue (0.134 g, 0.915 mmol) was dissolved in CH3CN (1.83 ml) and added to a solution of 3-(2,5-dichloro-3-methoxyphenyl)-pyridine-2,6-diamine (Preparation 4, 0.200 g, 0.704 mmol) in anhydrous pyridine (10 ml). The reaction was heated at 60° C. for 24 hours. A further 0.88 equivalents of the acid chloride in CH3CN (0.091 g, in 1.2 ml) was added and the reaction stirred for a further 24 hours at 60° C. The reaction was partitioned between dichloromethane and a saturated aqueous solution of NaHCO3 before drying over Na2SO4 and concentrating in vacuo. The residue was purified by silica gel column chromatography eluting with 5:95 to 30:70 ethyl acetate:heptane to afford the title compound (0.050 g, 18% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08134007B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-46100b110fba4c5cba629e80ff367c95
출처 메모uspto-grants-2012_03