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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 261450생성일: 2026년 10월 27일

Indomethacin → 1-(p-Chlorobenzoyl)-2-methyl-5-methoxy-3-indolylacetic acid-3-pyridylmethyl ester

https://huagongshe.com/reaction/261450

반응식

참여 물질

역할이름HCID투입량
반응물IndomethacinHCID 3715—
반응물3-PyridinemethanolHCID 7510—
반응물TriethylamineHCID 8471—
반응물Thionyl ChlorideHCID 24386—
용매BenzeneHCID 241—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물1-(p-Chlorobenzoyl)-2-methyl-5-methoxy-3-indolylacetic acid-3-pyridylmethyl esterHCID 2039505079.7%

반응 단계

A mixture of 3.0 g of 1-(p-chlorobenzoyl)-2-methyl-5-methoxy-3-indolylacetic acid and 3.0 g of thionyl chloride was refluxed in 70 ml of benzene for 3 hours. After cooling, the solvent was distilled off under reduced pressure to leave a residue. The residue was dissolved in 20 ml of tetrahydrofuran. This solution was added to a solution of 1.0 g of 3-pyridylmethanol in 70 ml of tetrahydrofuran under cooling. To this mixture was carefully added 0.95 g of triethylamine and stirring was continued for 2 hours at room temperature. After the reaction was complete, the solvent was removed by distillation under reduced pressure to leave a residue. After addition of water to the residue, an oily substance was obtained and extracted with chloroform. The extract was applied on a column of silica gel and the adsorbate was eluted with ether to give crystals. Recrystallization of the crystals from a mixed solvent of ethyl acetate ester and ether yielded 3.0 g of 1-(p-chlorobenzoyl)-2-methyl-5-methoxy-3-indolylacetic acid-3 -pyridylmethyl ester, melting at 116°-118° C. Analysis--Calculated for C25H21ClN2O4 : C, 66.89; H, 4.72; N, 6.24. Found: C, 67.06; H, 4.68; N, 6.11.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04165428
출처 데이터셋uspto-grants-1979_08
ORD IDord-56bb7ac1f25a47bc819591a99a670915
출처 메모uspto-grants-1979_08