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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223249Generated: October 26, 2026

Triethylamine → 2-[2-(3,5-Difluoro-benzylcarbamoyl)-propionylamino]-3-(1H-indol-3-yl)-propionic acid tert-butyl ester

https://huagongshe.com/reaction/2223249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant(S)-tert-butyl 2-amino-3-(1H-indol-3-yl)propanoate hydrochlorideHCID 11514895—
ReactantN-(3,5-difluoro-benzyl)-2-methyl-malonamic acidHCID 21091473—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-[2-(3,5-Difluoro-benzylcarbamoyl)-propionylamino]-3-(1H-indol-3-yl)-propionic acid tert-butyl esterHCID 69283610—

Reaction Steps

N-(3,5-Difluoro-benzyl)-2-methyl-malonamic acid (3.00 g, 12.3 mmol), L-tryptophan-tert-butylester hydrochloride (3.66 g, 12.3 mmol), TBTU (O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium-tetrafluoroborate, 3.96 g, 12.3 mmol) and triethylamin (3.74 g, 3.70 mmol) were dissolved in DMF (15 ml) and stirred for 5 h at r.t. The reaction mixture was poured into water and the product mixture was extracted with ethyl acetate. The organic layers were dried (Na2SO4). After evaporation of the solvent, the title compound, MS: m/e=486.4 (M+H+), (6.45 g, quant.) was obtained by chromatographic purification of the residue (silica gel, MeOH, CH2Cl2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375099B2
Source datasetuspto-grants-2008_05
ORD IDord-f9af4bff7cd243e6b0e6963277ceaea3
Source noteuspto-grants-2008_05