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HRID 2244963作成日:2026年10月27日

1,2-Dichloroethane → N-[4-(1-methyl-4,5-dihydro-1H-imidazol-2-yl)phenyl]-2-(1,1-dimethylethyl)-2-(4-chlorophenylaminocarbonylamino)-acetamide

https://huagongshe.com/reaction/2244963

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-Chlorophenyl IsocyanateHCID 7693—
反応物2-Amino-3,3-dimethylbutanoic acidHCID 306131—
反応物4-(1-Methyl-4,5-dihydro-1H-imidazol-2-yl)-phenylamineHCID 22728876—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物N-[4-(1-methyl-4,5-dihydro-1H-imidazol-2-yl)phenyl]-2-(1,1-dimethylethyl)-2-(4-chlorophenylaminocarbonylamino)-acetamideHCID 1154671224%

反応手順

To a solution of DL-tert-leucine (43 mg, 0.33 mmol) in DMF (2 mL), 4-chlorophenyl isocyanate (50 mg, 0.33 mmol) was added. The mixture was then stirred at room temperature overnight. To the reaction mixture, 4-(1-Methyl-4,5-dihydro-1H-imidazol-2-yl)-phenylamine (150 mg, 0.86 mmol) and H2O (0.5 mL, to solubilize the amine) were added. To the solution, EDC (127 mg, 0.66 mmol) was added. After being stirred at room temperature overnight, the solution was concentrated in vacuo. The residue was purified by HPLC to give the titled compound as a powder (35 mg). MS 442.1 and 444.1 (M+H, Cl pattern).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07678913B2
出典データセットuspto-grants-2010_03
ORD IDord-0dcef1a7a5ff4d948de1d9ca9bc7c4e7
出典メモuspto-grants-2010_03