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HRID 75243作成日:2026年10月24日

(2,6-Dichlorophenyl)hydrazine monohydrochloride → 2-(2,6-Dichlorophenyl)-2,8-dihydropyrazolo[3,4-d]dipyrido[2,3-b:3',4'-f]azepine

https://huagongshe.com/ja/reaction/75243

反応式

関与物質

役割名称HCID仕込み量
反応物(2,6-Dichlorophenyl)hydrazine monohydrochlorideHCID 2723909—
反応物6-[(Dimethylamino)methylene]-6,11-dihydro-5H-dipyrido[2,3-b: 3',4'-f]azepin-5-oneHCID 66886583—
溶媒EthanolHCID 702—
生成物2-(2,6-Dichlorophenyl)-2,8-dihydropyrazolo[3,4-d]dipyrido[2,3-b:3',4'-f]azepineHCID 135410898—

反応手順

(2,6-Dichlorophenyl)hydrazine hydrochloride (168 mg, 0.788 mmol) was added to a solution of 6-[(dimethylamino)methylene]-6,11-dihydro-5H-dipyrido[2,3-b:3′,4′-f]azepin-5-one (105 mg, 0.394 mmol, Intermediate E-1) in ethanol (4 mL) and stirred at room temperature. After 30 minutes, the mixture was heated to 60° C. overnight. The reaction was then cooled to room temperature and the major product from the reaction mixture was isolated using preparative LC/MS to provide the desired product as a white powder. 1H NMR (DMSO-d6) δ 8.77 (bs, 1H), 8.45 (bs, 1H), 8.40 (bs, 1H), 8.04 (m, 2H), 7.94 (d, 1H), 7.75 (m, 2H), 7.62 (m, 1H), 6.95 (m, 1H), 6.87 (m, 1H). LC/MS: 380 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835423B2
出典データセットuspto-grants-2014_09
ORD IDord-c99d50956acb4fe0b69453b7d8b919c8
出典メモuspto-grants-2014_09