戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1846749作成日:2026年10月26日

Diisopropylethylamine → 2-((1R,2S)-2-aminocyclohexylamino)-4-(1-methyl-1H-indol-4-ylamino)pyrimidine-5-carboxamide

https://huagongshe.com/reaction/1846749

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物2-(1H-benzo[d][1,2,3]triazol-1-yloxy)-4-(1-methyl-1H-indol-4-ylamino)pyrimidine-5-carboxamideHCID 57472013—
反応物butyl (1S,2R)-2-aminocyclohexylcarbamateHCID 57472014—
生成物2-((1R,2S)-2-aminocyclohexylamino)-4-(1-methyl-1H-indol-4-ylamino)pyrimidine-5-carboxamideHCID 5747201122.1%

反応条件

温度80 °C

反応手順

To a solid of 2-(1H-benzo[d][1,2,3]triazol-1-yloxy)-4-(1-methyl-1H-indol-4-ylamino)pyrimidine-5-carboxamide (100 mg, 0.25 mmol) in vial was added ten butyl (1S,2R)-2-aminocyclohexylcarbamate (0.3 M solution in NMP, 1.25 mL, 0.375 mmol) and DIPEA (0.09 mL, 0.5 mmol). It was heated at 80° C. for 2 h, cooled and purified by preparative HPLC to give 2-((1R,2S)-2-aminocyclohexylamino)-4-(1-methyl-1H-indol-4-ylamino)pyrimidine-5-carboxamide (21 mg). MS found for C20H25N2O as (M+H)+ 380.4. UV: λ=219.2, 241.6, 336.7.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08952027B2
出典データセットuspto-grants-2015_02
ORD IDord-33408eb028864036919deeccac002dd7
出典メモuspto-grants-2015_02