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HRID 220907作成日:2026年10月26日

4-Chloro-N-methylbenzenamine → 4-(3-{4-[(4-Chloro-phenyl)-methyl-carbamoyl]-2-fluoro-phenoxy}-propyl)-piperazine-1-carboxylic Acid Tert-butyl Ester

https://huagongshe.com/reaction/220907

反応式

関与物質

役割名称HCID仕込み量
反応物4-Chloro-N-methylbenzenamineHCID 70272—
反応物PyBroPHCID 2733179—
反応物4-[3-(4-Carboxy-2-fluoro-phenoxy)-propyl]-piperazine-1-carboxylic Acid Tert-butyl EsterHCID 57555209—
溶媒DichloromethaneHCID 6344—
溶媒DiisopropylethylamineHCID 81531—
生成物4-(3-{4-[(4-Chloro-phenyl)-methyl-carbamoyl]-2-fluoro-phenoxy}-propyl)-piperazine-1-carboxylic Acid Tert-butyl EsterHCID 5755527341%

反応手順

PyBroP (606 mg, 1.3 mmol) was added to a solution of 4-[3-(4-carboxy-2-fluoro-phenoxy)-propyl]-piperazine-1-carboxylic acid tert-butyl ester from Example E39 (382 mg, 11.0 mmol) in dichloromethane (20 ml) and DIEA (to pH9). The mixture was stirred for 1 h at room temperature then (4-chloro-phenyl)-methyl amine (156 mg, 1.1 mmol) was added. The mixture was stirred for 2 days at room temperature then solvents were concentrated in vacuo. The residue was dissolved in EtOAC, washed with saturated NaHCO3 then brine, dried and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (eluant; EtOAc) to yield the title compound (210 mg, 41%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08202858B2
出典データセットuspto-grants-2012_06
ORD IDord-59342acd21c4412db3be6a29284765f2
出典メモuspto-grants-2012_06