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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661791Generated: November 1, 2026

1-Hydroxybenzotriazole → 3-(R)-Azido-2-(S)-[(4'-ethyl-biphenyl-4-carbonyl)-amino]-butyric acid methyl ester

https://huagongshe.com/reaction/661791

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant4'-ethyl-4-biphenylcarboxylic acidHCID 521801—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant(2S,3R)-2-amino-3-azido-butyric acid methylester hydrochlorideHCID 86643747—
SolventDichloromethaneHCID 6344—
SolventEthyl acetate hexaneHCID 21226206—
Product3-(R)-Azido-2-(S)-[(4'-ethyl-biphenyl-4-carbonyl)-amino]-butyric acid methyl esterHCID 5969722767%

Reaction Steps

A EDC.HCl (249 mg, 1.3 mmol) was added to a stirred colorless solution of azido-Thr-OMe-HCl (4) (195 mg, 11.0 mmol), HOBT (158 mg, 11.0 mmol), 4′-Ethyl-biphenyl-4-carboxylic acid (5) (226 mg, 11.0 mmol) and DIEA (0.44 ml, 2.5 mmol) in DCM (10 ml) at rt under N2. After 24 h, the reaction had reached completion by TLC (Hexane/EtOAc (60:40) (Rf=0.3)) and LCMS. The reaction was evaporated under reduced pressure to a brown tar. The crude product was dissolved in EtOAc (100 ml) and washed with 0.2 N aq. HCl (2×50 ml), aq. sat. NaHCO3 (50 ml), brine (50 ml), dried (Na2SO4), filtered and concentrated under reduced pressure to yield a crude brown solid. The crude material was further purified by column chromatography eluting with Hexane/EtOAc (70:30) giving 245 mg (67% yield) of pure product after evaporation and drying in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084615B2
Source datasetuspto-grants-2011_12
ORD IDord-3a4aaac1ffc04cf2adc75ac5b6ca2c03
Source noteuspto-grants-2011_12