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HRID 53545作成日:2026年10月23日

Piperidin-3-ylmethanol → 5,11-Dihydro-11-ethyl-2-[3-(hydroxymethyl)piperidin-1-yl]-4-methyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one

https://huagongshe.com/ja/reaction/53545

反応式

関与物質

役割名称HCID仕込み量
反応物Piperidin-3-ylmethanolHCID 107308—
反応物Dipyridodiazepinone deriv. 15HCID 463144—
生成物5,11-Dihydro-11-ethyl-2-[3-(hydroxymethyl)piperidin-1-yl]-4-methyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-oneHCID 19960019—

反応手順

The title compound, m.p. 194°-197° C., was synthesized from 2-chloro-5,11-dihydro-11l-ethyl-4-methyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one and 3-piperidinemethanol using procedures analogous to those described above, except that the mixture was heated at 170°-180° C. for 2.5 hrs, and the product was crystallized from ethyl acetate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05620974
出典データセットuspto-grants-1997_04
ORD IDord-86d277589fbe4f28b104e3eb723a4307
出典メモuspto-grants-1997_04