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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19616생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/19616

반응식

참여 물질

역할이름HCID투입량
반응물P-PhenylenediamineHCID 7814—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물4-(((tert-Butoxycarbonyl)amino)methyl)benzoic acidHCID 853605—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
용매DimethylformamideHCID 6228—
용매TriethylamineHCID 8471—
생성물[4-(4-Amino-phenylcarbamoyl)-benzyl]-carbamic acid tert-butyl esterHCID 6731918955%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745446B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-8d3603ac7c024e62b278797a849ef08e
출처 메모uspto-grants-2010_06