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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415679Generated: October 25, 2026

Diphosgene → Benzyl 3-(3-isocyanatobenzamido)propionate

https://huagongshe.com/reaction/1415679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphosgeneHCID 10426—
ReactantDiisopropylethylamineHCID 81531—
Reactant3,5-Dimethyl-1H-pyrazole-1-carboxamidine mononitrateHCID 198186—
ReactantBenzyl 3-(3-aminobenzamido)propionateHCID 10424766—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductBenzyl 3-(3-isocyanatobenzamido)propionateHCID 54246722—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05908843
Source datasetuspto-grants-1999_06
ORD IDord-4a4fb0882bba4ccdb1bd050561552abc
Source noteuspto-grants-1999_06