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HRID 855424作成日:2026年10月25日

Dichloromethane → 6-Fluoro-1H-indole-7-carboxylic acid (4-tert-butyl-benzyl)-[2-(4-fluoro-phenyl)-ethyl]-amide

https://huagongshe.com/reaction/855424

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物6-fluoro-1H-indole-7-carboxylic AcidHCID 11708161—
反応物(4-Tert-butyl-benzyl)-[2-(4-fluoro-phenyl)-ethyl]-amineHCID 29280418—
生成物6-Fluoro-1H-indole-7-carboxylic acid (4-tert-butyl-benzyl)-[2-(4-fluoro-phenyl)-ethyl]-amideHCID 8660310938.1%

反応手順

To a solution of 59 mg (0.33 mmol) of 6-fluoro-1H-indole-7-carboxylic acid and 86 mg (0.3 mmol) of (4-tert-butyl-benzyl)-[2-(4-fluoro-phenyl)-ethyl]-amine in 3 ml DCM 63 mg (0.33 mmol) of EDC.HCl were added and the reaction mixture was stirred over night at rt. The product was purified by column chromatography (20 g silica gel; heptane/EtOAc 4:1) to yield 51 mg (38%) product as a colorless viscous oil. MS (ISP) 447.4 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07259183B2
出典データセットuspto-grants-2007_08
ORD IDord-69faf60e4f0d49baadecff25c4345da2
出典メモuspto-grants-2007_08