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HRID 851185作成日:2026年10月26日

3,4,5-Trimethoxyphenol → 1,2,3,4-Tetrahydro-8,9,10-trimethoxy-5H-[1]benzopyrano[3,4-c]pyridin-5-one hydrochloride

https://huagongshe.com/reaction/851185

反応式

関与物質

役割名称HCID仕込み量
反応物3,4,5-TrimethoxyphenolHCID 69505—
反応物Methyl 4-oxopiperidine-3-carboxylate hydrochlorideHCID 2724028—
生成物1,2,3,4-Tetrahydro-8,9,10-trimethoxy-5H-[1]benzopyrano[3,4-c]pyridin-5-one hydrochlorideHCID 1313691455%

反応手順

Prepared by the method described in Example 1 from 3,4,5-trimethoxyphenol (25 g, 0.14 moles) and methyl 4-oxo-3-piperidinecarboxylate hydrochloride (18.8 g, 0.097 moles). Recrystallization from dilute aqueous hydrochloric acid yielded the product (17.5 g) as the hydrochloride, mp 232°-234° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04382939
出典データセットuspto-grants-1983_05
ORD IDord-32bc5c3456fd4bc0b985babfe6c8a89f
出典メモuspto-grants-1983_05