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HRID 597050作成日:2026年10月26日

Levulinic Acid → 2-Methyl-5-methoxy-1-(7-chloroquinazolin-4-yl)indol-3-ylacetic acid monohydrate

https://huagongshe.com/reaction/597050

反応式

関与物質

役割名称HCID仕込み量
反応物Levulinic AcidHCID 11579—
反応物acetaldehyde N1-(7-chloroquinazolin-4-yl)p-methoxyphenylhydrazone hydrochlorideHCID 86734555—
溶媒WaterHCID 962—
生成物2-Methyl-5-methoxy-1-(7-chloroquinazolin-4-yl)indol-3-ylacetic acid monohydrateHCID 86734554—

反応手順

A mixture of laevulinic acid (15g.) and acetaldehyde N1 -(7-chloroquinazolin-4-yl)-p-methoxyphenylhydrazone hydrochloride (3.3g.) was heated at 95°-100° C. for 18 hours. The mixture was poured into water (ca 300ml.), and the precipitated pale yellow solid was collected by filtration and dissolved in a mixture of water (80ml.) and ammonia solution (specific gravity 0.88, ca 5ml.). The solution was washed with ethyl acetate (2 × 25ml.). Addition of sodium chloride (ca 10g.) to the aqueous phase caused a yellow solid to precipitate. This was collected by filtration, and then dissolved in water. The solution was acidified with glacial acetic acid until precipitation was complete. The mixture was filtered to give, as solid residue, 2-methyl-5-methoxy-1-(7-chloroquinazolin-4-yl)indol-3-ylacetic acid monohydrate, m.p. 98°-100° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04012513
出典データセットuspto-grants-1977_03
ORD IDord-157e2c242f784cbaac7562b73481385d
出典メモuspto-grants-1977_03