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HRID 491633作成日:2026年10月26日

1,2-Dichloroethane → HCID 178485437、化合物

https://huagongshe.com/reaction/491633

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HCID 17755843HCID 17755843—
反応物3-(3,4-Diamino-phenoxy)-N-methyl-benzamideHCID 69017151—
溶媒AcetonitrileHCID 6342—
生成物HCID 178485437HCID 178485437—

反応手順

3-(3,4-Diamino-phenoxy)-N-methyl-benzamide (Step C, 400 mg, 1.5 mmol, 1.0 eq.) was dissolved in anh. CH3CN (10 mL) and a solution of 1-(2-chloro-5-isothiocyanato-benzyl)-4-methyl-piperazine (330 mg, 1.2 mmol, 0.8 eq.) in CH3CN (10 mL) was added dropwise. The reaction was stirred at RT for 2 h. EDC (240 mg, 1.3 mmol, 0.9 eq.) was added, the mixture was heated to 80° C. and stirred for 2 h. The CH3CN was evaporated and the crude compound was dissolved in CH2Cl2, washed with water and sat. NaHCO3 (aq.). The organic layer was dried (MgSO4), filtered and concentrated. Further purification by column chromatography (0-10% EtOH/CH2Cl2, two runs were required) gave pure 3-{2-[4-chloro-3-(4-methyl-piperazin-1-ylmethyl)-phenylamino]-1H-benzimidazol-5-yloxy}-N-methyl-benzamide. MS m/z=505.2 (M+H)+; MW Calc'd for C27H29N6O2: 504.20.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07531553B2
出典データセットuspto-grants-2009_05
ORD IDord-17a3d6edc86b4a7bb09132746d3ea342
出典メモuspto-grants-2009_05