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HRID 19616作成日:2026年10月26日

P-Phenylenediamine → [4-(4-Amino-phenylcarbamoyl)-benzyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/19616

反応式

関与物質

役割名称HCID仕込み量
反応物P-PhenylenediamineHCID 7814—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物4-(((tert-Butoxycarbonyl)amino)methyl)benzoic acidHCID 853605—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
溶媒DimethylformamideHCID 6228—
溶媒TriethylamineHCID 8471—
生成物[4-(4-Amino-phenylcarbamoyl)-benzyl]-carbamic acid tert-butyl esterHCID 6731918955%

反応手順

To a solution of 4-(tert-butoxycarbonylamino-methyl)-benzoic acid (1.005 g) and N-hydroxy-benzotriazole (HOBt)(0.642 g) in DMF (30 ml) are added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC)(2.76 g) and triethylamine (2.005 ml). The mixture is stirred for 1 h at ambient temperature. This solution is added at 0° C. slowly to a solution of 1,4-diaminobenzene (0.43 g) and triethylamine (0.45 ml) in DMF (5 ml). After completion of the chemical reaction the mixture is evaporated at high vacuum and the residue is partitioned between ethyl acetate and an aqueous saturated sodium bicarbonate solution. The organic phase is dried over sodium sulfate and the crude product is purified by silica gel flash chromatography. A colorless solid (0.735 g) is obtained in 55% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745446B2
出典データセットuspto-grants-2010_06
ORD IDord-8d3603ac7c024e62b278797a849ef08e
出典メモuspto-grants-2010_06