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HRID 1432543作成日:2026年10月25日

1,2-Dichloroethane → N-[4-(3-thiazolidinylcarbonyl)phenyl]-2N-(4-chlorophenylaminocarbonyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxamide

https://huagongshe.com/reaction/1432543

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物4-(3-Thiazolidinylcarbonyl)phenylamineHCID 68693033—
反応物(4-Chlorophenylaminocarbonyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acidHCID 131727716—
溶媒DimethylformamideHCID 6228—
生成物N-[4-(3-thiazolidinylcarbonyl)phenyl]-2N-(4-chlorophenylaminocarbonyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxamideHCID 1159885481.9%

反応手順

To a solution of 2N-(4-chlorophenylaminocarbonyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (50 mg, 0.15 mmol) and 4-(3-thiazolidinylcarbonyl)phenylamine (30 mg, 0.14 mmol) in DMF (2 mL), EDC (54 mg, 0.28 mmol) was added. The reaction mixture was stirred at room temperature overnight. It was then concentrated in vacuo. The residue was purified by HPLC to give the titled compound as a white powder (32 mg). MS 521.0 and 523.0 (M+H, Cl pattern).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07612089B2
出典データセットuspto-grants-2009_11
ORD IDord-b97b82cbcf0c4f648f987c320d1f557f
出典メモuspto-grants-2009_11