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HRID 1956449作成日:2026年10月25日

Hydrochloric Acid → Ethyl 4-(6-ethoxy-3-ethoxycarbonyl-7-methyl-1,8-naphthyridin-4-ylamino)phenoxyacetate hydrochloride

https://huagongshe.com/reaction/1956449

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物(4-Nitrophenoxy)acetic acidHCID 15720—
反応物Ethyl 4-chloro-6-ethoxy-7-methyl-1,8-naphthyridine-3-carboxylateHCID 23198600—
反応物2-(4-Aminophenoxy)acetic acid hydrochlorideHCID 66811488—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
生成物Ethyl 4-(6-ethoxy-3-ethoxycarbonyl-7-methyl-1,8-naphthyridin-4-ylamino)phenoxyacetate hydrochlorideHCID 23209201—

反応手順

A mixture of ethyl 4-chloro-6-ethoxy-7-methyl-1,8-naphthyridine-3-carboxylate (3.1 g), 4-aminophenoxy-acetic acid hydrochloride (2.17 g) (prepared by reduction of 4-nitrophenoxyacetic acid using hydrogen and 10% palladium charcoal in a similar manner to Example C1 followed by treatment with 5M hydrochloric acid and then evaporation) and absolute ethanol (30 ml) was boiled under reflux for 4 hours. The mixture was cooled to ambient temperature and filtered to give ethyl 4-(6-ethoxy-3-ethoxycarbonyl-7-methyl-1,8-naphthyridin-4-ylamino)phenoxyacetate hydrochloride, m.p. 192°-194° C. Active (1/1) at 30 mg/kg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05780482
出典データセットuspto-grants-1998_07
ORD IDord-37e46e3a8e6e4262905661911104d076
出典メモuspto-grants-1998_07