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HRID 1992739作成日:2026年10月24日

Trifluoroacetic acid → 3,5-Dibromo-N-(2-methyl-3-phenyl-allyl)-N-[2-(1-methyl-pyrrolidin-2-yl)-ethyl]-benzamide

https://huagongshe.com/ja/reaction/1992739

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物Benzoic acid, 3,5-dibromo-HCID 12063—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物(2-Methyl-3-phenyl-allyl)-[2-(1-methyl-pyrrolidin-2-yl)-ethyl]-amineHCID 68680591—
溶媒AcetonitrileHCID 6342—
溶媒TriethylamineHCID 8471—
生成物3,5-Dibromo-N-(2-methyl-3-phenyl-allyl)-N-[2-(1-methyl-pyrrolidin-2-yl)-ethyl]-benzamideHCID 6868272363%

反応手順

An analogous procedure to Example 2 was used with 3,5-dibromo-benzoic acid 0.16 g (0.38 mmol) and (2-methyl-3-phenyl-allyl)-[2-(1-methyl-pyrrolidine-2-yl)-ethyl]-amine 0.1 g (0.38 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride 0.11 g (0.57 mmol), 1-hydroxybenzotriazole 0.05 g (0.41 mmol) and triethylamine 0.08 ml. Reverse phase prep HPLC with a gradient 20-80% for the acetonitrile phase gavel 53 mg as a TFA salt. Yield: 63%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07649011B2
出典データセットuspto-grants-2010_01
ORD IDord-35fdc6c84df143be8e1de87b274c755c
出典メモuspto-grants-2010_01