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HRID 1005作成日:2026年10月23日

4-(1,4-Dioxaspiro[4.5]dec-8-ylamino)-3-methoxy-2-methylpyridine hydrochloride → 4-(4-Oxocyclohexylamino)-3-methoxy-2-methylpyridine hydrochloride

https://huagongshe.com/ja/reaction/1005

反応式

関与物質

役割名称HCID仕込み量
反応物4-(1,4-Dioxaspiro[4.5]dec-8-ylamino)-3-methoxy-2-methylpyridine hydrochlorideHCID 19694011—
溶媒Formic AcidHCID 284—
生成物4-(4-Oxocyclohexylamino)-3-methoxy-2-methylpyridine hydrochlorideHCID 19693963—

反応手順

27.3 g of 4-(1,4-dioxaspiro[4.5]dec-8-ylamino)-3-methoxy-2-methylpyridine hydrochloride are stirred with 400 ml of formic acid for 4 hours. The residue which remains after concentrating in vacuo is dissolved in methylene chloride and shaken with 2N NaOH. The methylene chloride phase is concentrated, the residue is dissolved in ether and the hydrochloride is precipitated by addition of ethereal HCl. 14 g=90%; m.p.: 115° to 120° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723450
出典データセットuspto-grants-1998_03
ORD IDord-87cd3f597261426bbf9068b66cd80964
出典メモuspto-grants-1998_03