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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1415679Erstellt: 26. Oktober 2026

Diphosgene → Benzyl 3-(3-isocyanatobenzamido)propionate

https://huagongshe.com/reaction/1415679

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiphosgeneHCID 10426—
EduktDiisopropylethylamineHCID 81531—
Edukt3,5-Dimethyl-1H-pyrazole-1-carboxamidine mononitrateHCID 198186—
EduktBenzyl 3-(3-aminobenzamido)propionateHCID 10424766—
LösungsmittelWaterHCID 962—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktBenzyl 3-(3-isocyanatobenzamido)propionateHCID 54246722—

Reaktionsschritte

0.17 ml of ethyldiisopropylamine is added to a solution of 201 mg of 1-amidino-3,5-dimethylpyrazole nitrate in 17 ml of dioxane and 5 ml of water and the mixture is stirred for 15 minutes. 357 mg of 3-(3-(piperazin-1-ylcarboxamido)benzamido)propionic acid hydrochloride (FAB 321; obtainable by reacting benzyl 3-(3-aminobenzamido)propionate with diphosgene to give benzyl 3-(3-isocyanatobenzamido)propionate, adding on 1-BOC-piperazine to give benzyl 3-(3-(4-BOC-piperazin-1-ylcarboxamido)benzamido)propionate, cleaving the BOC group with 4 N HCl in dioxane to give benzyl 3-(3-(piperazin-1-ylcarboxamido)benzamido)propionate hydrochloride (FAB 411) and hydrogenolyzing on 5% Pd/C) and a further 0.17 ml of ethyldiisopropylamine are then added, the mixture is boiled for 45 hours and evaporated, the residue is dissolved in water and the solution is washed with ether and then with ethyl acetate and evaporated again to give 3-(3-(4-amidinopiperazin-1-ylcarboxamido)benzamido)propionic acid, m.p. 234° (decomposition).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05908843
Quelldatensatzuspto-grants-1999_06
ORD IDord-4a4fb0882bba4ccdb1bd050561552abc
Quellennotizuspto-grants-1999_06