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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885123Generated: November 1, 2026

Benzoic Acid → HCID 25106076, compound

https://huagongshe.com/reaction/885123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
Reactant4-MethylmorpholineHCID 7972—
ReactantSodium HydroxideHCID 14798—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantHCID 68720623HCID 68720623—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 25106076HCID 25106076—

Reaction Steps

A N,N-dimethylformamide (1 mL) solution of Example 24B (0.025 g, 0.079 mmol), benzoic acid (0.011 g, 0.087 mmol), 1-ethyl-3-[3-(dimethylamino)propyl]-carbodiimide hydrochloride (0.015 g, 0.079 mmol), 1-hydroxybenzotriazole hydrate (0.011 g, 0.079 mmol), and N-methylmorpholine (0.345 mL, 0.314 mmol) was heated to 55° C. for 16 h. The solution was cooled to room temperature and diluted with ethyl acetate (2 mL) and H2O (2 mL). The layers were separated, and the organic was washed with brine (1×1 mL), dried with anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue was dissolved in methanol (2 mL) and 2.5M NaOH (0.95 mL, 0.237 mmol) was added. The reaction was stirred at room temperature for 16 h, concentrated under reduced pressure, and purified by RP-HPLC (preparative reversed-phase high pressure liquid chromatography) using a Zorbax SB-C18 7M 21.2×250 mm column with UV detection analyzed at 220 and 254 nM (preparative method: water with 0.1% trifluoroacetic acid and CH3CN with 0.1% trifluoroacetic acid gradient 5-95% CH3CN over 30 minutes at 15 mL/min) to provide the title compound as a white solid. 1H NMR (300 MHz, METHANOL-d4) δ ppm 1.83-1.93 (m, 1H), 1.95-2105 (m, 1H), 2.53-2.67 (m, 5H), 3.99 (s, 2H), 7.49-7.60 (m, 4H), 7.63-7.67 (m, 2H) 7.81 (m, 2H), 7.92-7.94 (m, 2H), 7.97 (s, 1H); MS (ESI) m/z 409 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242139B2
Source datasetuspto-grants-2012_08
ORD IDord-1e7a82ffd50d4d4488efbd0bf25cbfec
Source noteuspto-grants-2012_08