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HRID 15318作成日:2026年10月26日

3-Oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]thiazine-6-carbaldehyde → 3-Chloro-4-[((3r,4s)-3-hydroxy-4-{[(3-oxo-3,4-dihydro-2h-pyrido[3,2-b][1,4]thiazin-6-yl)methyl]amino}-1-piperidinyl)methyl]-4,5-dihydro-7h-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one hydrochloride

https://huagongshe.com/reaction/15318

反応式

関与物質

役割名称HCID仕込み量
反応物3-Oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]thiazine-6-carbaldehydeHCID 11593591—
反応物racemic 4-{[(3R,4S)-4-amino-3-hydroxy-1-piperidinyl]methyl}-3-chloro-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-oneHCID 68685696—
生成物3-Chloro-4-[((3r,4s)-3-hydroxy-4-{[(3-oxo-3,4-dihydro-2h-pyrido[3,2-b][1,4]thiazin-6-yl)methyl]amino}-1-piperidinyl)methyl]-4,5-dihydro-7h-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one hydrochlorideHCID 6868525149%

反応手順

The free base of the title compound was synthesised from racemic 4-{[(3R,4S)-4-amino-3-hydroxy-1-piperidinyl]methyl}-3-chloro-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one and 3-oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]thiazine-6-carboxaldehyde (for a synthesis see WO2003087098, Example 301(d)) according to the general method of Example 2(h), in 49% yield.

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-abbd941e5ebe45fb83278a80418ace39
出典メモuspto-grants-2010_06