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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297385Generated: October 30, 2026

Diisopropylethylamine → tert-butyl (2S)-2-benzyloxycarbonylamino-3-(4-(2-methoxycarbonylethyl)benzoylamino)propionate

https://huagongshe.com/reaction/2297385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-[(Ethoxycarbonyl)cyanomethylenamino]-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733286—
Reactant(S)-tert-Butyl 3-amino-2-(((benzyloxy)carbonyl)amino)propanoateHCID 10803731—
Reactant4-(3-Methoxy-3-oxopropyl)benzoic acidHCID 11310294—
SolventDimethylformamideHCID 6228—
Producttert-butyl (2S)-2-benzyloxycarbonylamino-3-(4-(2-methoxycarbonylethyl)benzoylamino)propionateHCID 15512203—

Reaction Steps

354 mg (1.7 mmol) of 4-(2-methoxycarbonylethyl)benzoic acid and 500 mg (1.7 mmol) of tert-butyl (2S)-3-amino-2-benzyloxycarbonylaminopropionate were dissolved in 3 ml of dimethylformamide and treated with 557 mg (1.7 mmol) of O-((cyano-(ethoxycarbonyl)-methylidene)amino)-1,1,3,3-tetramethyluronium tetrafluoroborate (TOTU) and 204 mg (1.7 mmol) of diisopropylethylamine and the mixture was stirred at room temperature for 7 h at pH 7-8. The solvent was removed in vacuo, the residue was dissolved in ethyl acetate and the solution was washed three times each with KHSO4 solution and NaHCO3 solution until neutral. The organic phase was separated off and dried and the solvent was removed by distillation in vacuo. Yield: 770 mg (93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492356B1
Source datasetuspto-grants-2002_12
ORD IDord-ae0174f7101e40bfacf278062e9dfe9e
Source noteuspto-grants-2002_12