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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2170006생성일: 2026년 10월 27일

3-Methylsalicylic Acid → 2-hydroxy-N-(6-methoxypyridin-2-yl)-3-methylbenzamide

https://huagongshe.com/reaction/2170006

반응식

참여 물질

역할이름HCID투입량
반응물3-Methylsalicylic AcidHCID 6738—
반응물SalicylaldehydeHCID 6998—
반응물Sodium HydroxideHCID 14798—
반응물Thionyl ChlorideHCID 24386—
반응물2-Amino-6-methoxypyridineHCID 580053—
용매PyridineHCID 1049—
용매Ethyl AcetateHCID 8857—
생성물2-hydroxy-N-(6-methoxypyridin-2-yl)-3-methylbenzamideHCID 67259030—

반응 조건

온도90 °C

반응 단계

10 ml of thionyl chloride are added to 1.47 g (16.11 mmol) of 2-hydroxy-3-methylbenzoic acid and the reaction mixture is heated at 90° C. for 2 h. The reaction medium is concentrated to dryness by azeotroping with toluene. The residue is then put into solution in 10 ml of pyridine, to which 600 mg (4.83 mmol, 1 eq) of 2 methoxypyridin-6-amine are added dropwise, and the reaction medium is left stirring at room temperature for 1 h 30 mins. 30 ml of 1M sodium hydroxide (19.34 mmol, 4 eq) are added and the reaction medium is heated at 60° C. for 16 h. The reaction medium is diluted with 100 ml of ethyl acetate, the aqueous phase is extracted and washed with 50 ml of ethyl acetate. The aqueous phase is then acidified at 0° C. with 37% HCl dropwise to pH=4. The organic phases are extracted twice with 50 ml of ethyl acetate and then they are washed twice with 50 ml of water. The organic phases are concentrated to dryness and the residue is purified by chromatography over silica, eluting with a heptane/ethyl acetate (1/1) mixture. 2-Hydroxy-N-(6-methoxypyridin-2-yl)-3-methylbenzamide is obtained in the form of a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09050266B2
출처 데이터셋uspto-grants-2015_06
ORD IDord-9a5f805baca24defa7cb54489d0b413c
출처 메모uspto-grants-2015_06