戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1612046作成日:2026年10月26日

Dimethylformamide → 2-Chloro-6H-thieno[2,3-b]pyrrole-5-carboxylic acid-[1-benzyl-2-methoxy-2-(methoxymethyl-carbamoyl)-ethyl]-amide

https://huagongshe.com/reaction/1612046

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物TriethylamineHCID 8471—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物2-Chloro-6H-thieno[2,3-b]pyrrole-5-carboxylic acidHCID 10442820—
反応物3-amino-2,N-dimethoxy-N-methyl-4-phenyl-butyramideHCID 22252947—
溶媒Ethyl AcetateHCID 8857—
生成物2-Chloro-6H-thieno[2,3-b]pyrrole-5-carboxylic acid-[1-benzyl-2-methoxy-2-(methoxymethyl-carbamoyl)-ethyl]-amideHCID 22252951—

反応手順

Triethylamine was added dropwise to a solution of 3-amino-2,N-dimethoxy-N-methyl-4-phenyl-butyramide (PCT International Application Publication No. WO 96/39385) (1.65 g, 5.71 mmol) in DMF (15 mL) and cooled in an ice bath. A solution of 2-chloro-6H-thieno[2,3-b]pyrrole-5-carboxylic acid (U.S. Pat. No. 6,399,601) (1.1 g, 5.71 mmol) in 15 mL of DMF was added dropwise followed by the addition of HOBT (1.16 g, 11.4 mmol) neat. The reaction mixture was stirred for 5 min and N-ethyliminomethylene-N,N′-dimethyl-propane-1,3-diamine (1.10 g, 5.71 mmol) was added neat. The resulting mixture was stirred at room temperature for 18 hrs. The reaction mixture was diluted with ethyl acetate (150 mL) and washed with saturated ammonium chloride, water, and brine. The ethyl acetate was dried and evaporated in vacuo to yield 2.54 g of crude product. Chromatography over silica gel, eluting with ethyl acetate/hexanes (1:2), afforded 1.43 g of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06992101B2
出典データセットuspto-grants-2006_01
ORD IDord-9c08440f20d54915aa9e7039f4f49833
出典メモuspto-grants-2006_01