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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724723Generated: October 30, 2026

Diisopropylethylamine → tert-Butyl (1S)-1-(3-bromo-4-iodobenzyl)-2-oxo-2-[(2-oxo-2-phenylethyl)amino]ethylcarbamate

https://huagongshe.com/reaction/724723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantEthanone, 2-amino-1-phenyl-, hydrochloride (1:1)HCID 2723597—
Reactant(2S)-3-(3-bromo-4-iodophenyl)-2-[(tert-butoxycarbonyl)amino]propanoic acidHCID 69597598—
SolventDimethylformamideHCID 6228—
SolventSodium BicarbonateHCID 516892—
Producttert-Butyl (1S)-1-(3-bromo-4-iodobenzyl)-2-oxo-2-[(2-oxo-2-phenylethyl)amino]ethylcarbamateHCID 5874657233.5%

Reaction Steps

A solution of (2S)-3-(3-bromo-4-iodophenyl)-2-[(tert-butoxycarbonyl)amino]propanoic acid (4.10 g, 6.10 mmol), N,N-dimethylformamide (49 mL) and benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (4.24 g, 9.59 mmol) was stirred at 25° C. After stirring for 10 min, added 2-amino-1-phenylethanone hydrochloride (2.24 g, 13.1 mmol) and N,N-diisopropylethylamine (7.60 mL). The reaction was stirred at 25° C. for 2 h. The reaction was diluted with saturated sodium bicarbonate and extracted with ethyl acetate three times, dried with sodium sulfate, filtered, and concentrated in vacuo. The crude residue was purified by flash column chromatography to yield the desired product (1.2 g, 33%). MF=C22H24BrIN2O4; LCMS found for C22H25BrIN2O4 (M+H−Boc)+: m/z=487.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141596B2
Source datasetuspto-grants-2006_11
ORD IDord-f4f35f990acf460e80d8137118181220
Source noteuspto-grants-2006_11