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HRID 597061생성일: 2026년 10월 26일

Water → 1-(7-Chloroquinazolin-4-yl)-5-methoxy-2-methylindol-3-ylacetic acid

https://huagongshe.com/reaction/597061

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Levulinic AcidHCID 11579—
반응물acetaldehyde N1-(7-chloroquinazolin-4-yl)p-methoxyphenylhydrazone hydrochlorideHCID 86734555—
용매Acetic AcidHCID 176—
생성물1-(7-Chloroquinazolin-4-yl)-5-methoxy-2-methylindol-3-ylacetic acidHCID 10194003—

반응 단계

A mixture of acetaldehyde N1 -(7chloroquinazolin-4-yl)-p-methoxyphenylhydrazone hydrochloride (25g.) and laevulinic acid (50g.) in acetic acid (120ml.) was heated under reflux for 1-2 hours. The dark red mixture was then added to water (1.5 1.). The solid obtained was separated by filtration and dissolved in a mixture of water (50ml.) and 5N-aqueous ammonium hydroxide solution (50ml.). The solution was extracted with ether (3 × 50ml.) and the aqueous layer acidified with acetic acid to pH4. The mixture was then extracted with ethyl acetate (3 × 50ml.) and the extracts washed with water (30ml.) and then with saturated sodium chloride solution (30ml.) before being dried (MgSO4). Evaporation of the solvent gave a dark brown syrup which crystallised on addition of methanol (40ml.) to give 1-(7-chloroquinazolin-4-yl)5-methoxy-2-methylindol-3-ylacetic acid as a yellow solid, m.p. 205°-208° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04012513
출처 데이터셋uspto-grants-1977_03
ORD IDord-e16c723d78704363889cb0d090861da9
출처 메모uspto-grants-1977_03