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HRID 15345作成日:2026年10月24日

[1,3]Oxathiolo[5,4-c]pyridine-6-carbaldehyde → 4-({4-[([1,3]oxathiolo[5,4-c]pyridin-6-ylmethyl)amino]-1-piperidinyl}methyl)-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one hydrochloride

https://huagongshe.com/ja/reaction/15345

反応式

関与物質

役割名称HCID仕込み量
反応物[1,3]Oxathiolo[5,4-c]pyridine-6-carbaldehydeHCID 59254367—
反応物4-[(4-Amino-1-piperidinyl)methyl]-4,5-dihydro-7h-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one dihydrochloride saltHCID 68685371—
生成物4-({4-[([1,3]oxathiolo[5,4-c]pyridin-6-ylmethyl)amino]-1-piperidinyl}methyl)-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one hydrochlorideHCID 68688399—

反応手順

The free base of the title compound was synthesised from 4-[(4-amino-1-piperidinyl)methyl]-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one dihydrochloride salt and [1,3]oxathiolo[5,4-c]pyridine-6-carbaldehyde (for a synthesis see WO2004058144, Example 61) according to the general method of Example 2(h).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732461B2
出典データセットuspto-grants-2010_06
ORD IDord-4a0006bc761c4184b305e3d17ebbb089
出典メモuspto-grants-2010_06