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HRID 14993作成日:2026年10月23日

5-Methoxy[1,3]thiazolo[5,4-b]pyridin-2-amine → N-(5-methoxythiazolo[5,4-b]pyridin-2-yl)-2-(10-methyl-5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-3-((R)-3-oxocyclopentyl)propionamide

https://huagongshe.com/ja/reaction/14993

反応式

関与物質

役割名称HCID仕込み量
反応物5-Methoxy[1,3]thiazolo[5,4-b]pyridin-2-amineHCID 2801557—
反応物methyl (1S)-3-oxocyclopentane-1-carboxylateHCID 13827616—
反応物Ethyl (10-methyl-5,5-dioxo-5,10-dihydrophenothiazin-2-yl)acetateHCID 59340971—
反応物(S)-7-iodomethyl-1,4-d ioxaspiro[4.4]nonaneHCID 67237087—
生成物N-(5-methoxythiazolo[5,4-b]pyridin-2-yl)-2-(10-methyl-5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-3-((R)-3-oxocyclopentyl)propionamideHCID 86637550—

反応手順

Analogously to Example 1 and Example 36, ethyl (10-methyl-5,5-dioxo-5,10-dihydrophenothiazin-2-yl)acetate, (S)-7-iodomethyl-1,4-d ioxaspiro[4.4]nonane (prepared analogously to Example 40 from commercially available methyl (S)-3-oxo-cyclopentanecarboxylate) and 5-methoxy-thiazolo[5,4-b]pyridin-2-ylamine give N-(5-methoxythiazolo[5,4-b]pyridin-2-yl)-2-(10-methyl-5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-3-((R)-3-oxocyclopentyl)propionamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732440B2
出典データセットuspto-grants-2010_06
ORD IDord-21acdf692c1a49009e3af8ed3e8a6972
出典メモuspto-grants-2010_06