戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 548012作成日:2026年10月23日

Tris(hydroxymethyl)aminomethane → N-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)benzo[d][1,3]dioxole-5-carboxamide

https://huagongshe.com/ja/reaction/548012

反応式

関与物質

役割名称HCID仕込み量
反応物Tris(hydroxymethyl)aminomethaneHCID 6503—
反応物1,3-Benzodioxole-5-carboxylic acidHCID 7196—
反応物1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-amine hydrochlorideHCID 57422264—
反応物HCID 178418300HCID 178418300—
溶媒DimethylformamideHCID 6228—
溶媒AcetonitrileHCID 6342—
生成物N-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)benzo[d][1,3]dioxole-5-carboxamideHCID 574222676%

反応手順

1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-amine hydrochloride (example 1a) (8 mg, 35 μmol) and benzo[d][1,3]dioxole-5-carboxylic acid (7 mg, 42 μmol) were each dissolved in 200 uL dimethylformamide. Si-Carbodiimide resin (70 mg, 70 μmol) was loaded into a 1.2 mL 96 well Greiner plate, followed by the addition of amine and acid. Hydroxybenzotriazole (6 mg, 42 μmol) was dissolved in 100 uL dimethylformamide and was added into the reaction well. The reaction was shaken overnight at room temperature. To remove excess carboxylic acid and hydroxybenzotriazole, PS-Trisamine resin (35 mg, 70 μmol) was added into the reaction mixture and was allowed to shake overnight at room temperature. 200 uL of Acetonitrile was added into the reaction well and shaken for 1 minute. The top clear solution was transferred into a new plate. The extraction process was repeated two more times. The solution was evaporated under vacuum and gave the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07939671B2
出典データセットuspto-grants-2011_05
ORD IDord-fa1f933f40374b9985f64408d40ba93c
出典メモuspto-grants-2011_05