Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422339Generated: October 31, 2026

1-Hydroxybenzotriazole → 5-Fluoro-4-hydroxy-3-{2-[(1H-imidazole-2-carbonyl)-amino]-propionylamino}-pentanoic acid tert-butyl ester

https://huagongshe.com/reaction/2422339

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3-Amino-5-fluoro-4-hydroxy-pentanoic acid tert-butyl esterHCID 10856672—
Reactant(2S)-2-[(1H-imidazole-2-carbonyl)-amino]-propionic acidHCID 57462012—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
Product5-Fluoro-4-hydroxy-3-{2-[(1H-imidazole-2-carbonyl)-amino]-propionylamino}-pentanoic acid tert-butyl esterHCID 6705872097%

Reaction Steps

A solution of (2S)-2-[(1H-imidazole-2-carbonyl)-amino]-propionic acid and 3-amino-5-fluoro-4-hydroxy-pentanoic acid tert-butyl ester (0.254 g) in THF (7 mL) was cooled to 0° C. before addition of DMAP (0.151 g), diisopropylethyl amine (0.56 mL), HOBT (0.16 g) and EDC HCl (0.23 g). The reaction mixture was stirred at ambient temperature for 18 hrs before being concentrated at reduced pressure. The residue was purified by silica gel chromatography (5% methanol in dichloromethane) to afford the sub-title compound as a colourless solid (0.386 g, 97%): 1H NMR 400 MHz CDCl3/CD3OD 1.40 (12H, m), 3.92 (1H, m), 4.20-4.55 (4H, m), 7.11 (2H, d, J 15); 19F NMR CDCl3−229.74 (m), −229.84 (m), −230.54 (m), −230.87 (m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960398B2
Source datasetuspto-grants-2011_06
ORD IDord-198dcc8cb72c4318a087693049e83de7
Source noteuspto-grants-2011_06