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HRID 2299306作成日:2026年10月26日

N-(4-chlorobenzyl)-7-methyl-2-(4-morpholinylmethyl)-4-oxo-4,7-dihydrothieno(2,3-b)pyridine-5-carboxamide → Thieno(2,3-b)pyridine-5-carboxamide, N-((4-chlorophenyl)methyl)-4,7-dihydro-7-methyl-2-(4-morpholinylmethyl)-4-oxo-, hydrochloride (1:1)

https://huagongshe.com/reaction/2299306

反応式

関与物質

役割名称HCID仕込み量
反応物N-(4-chlorobenzyl)-7-methyl-2-(4-morpholinylmethyl)-4-oxo-4,7-dihydrothieno(2,3-b)pyridine-5-carboxamideHCID 503580—
溶媒Hydrochloric AcidHCID 313—
生成物Thieno(2,3-b)pyridine-5-carboxamide, N-((4-chlorophenyl)methyl)-4,7-dihydro-7-methyl-2-(4-morpholinylmethyl)-4-oxo-, hydrochloride (1:1)HCID 18380160179.3%

反応手順

N-(4-chlorobenzyl)-7-methyl-2-(4-morpholinylmethyl)-4-oxo-4,7-dihydro-thieno[2,3-b]pyridine-5-carboxamide (1.50 g) from Example No. 36 is dissolved in methanolic HCl (50 mL) and concentrated in vacuo. The resulting off-white solid is recrystallized from methanol/ethanol to yield 1.458 g (90%) of the title compound as a white solid. Physical characteristics are as follows:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06495683B2
出典データセットuspto-grants-2002_12
ORD IDord-df221610b9cd49ada947e9d0dbd21160
出典メモuspto-grants-2002_12