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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19616Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktP-PhenylenediamineHCID 7814—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt4-(((tert-Butoxycarbonyl)amino)methyl)benzoic acidHCID 853605—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTriethylamineHCID 8471—
Produkt[4-(4-Amino-phenylcarbamoyl)-benzyl]-carbamic acid tert-butyl esterHCID 6731918955%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745446B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-8d3603ac7c024e62b278797a849ef08e
Quellennotizuspto-grants-2010_06