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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1513233Generated: October 27, 2026

Triethylamine → 4-Chloro-benzoic acid N'-(4-amino-3-nitro-benzoyl)-hydrazide

https://huagongshe.com/reaction/1513233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-ChlorobenzohydrazideHCID 10816—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantBenzoic acid, 4-amino-3-nitro-HCID 74115—
Reactant1-HydroxybenzotriazoleHCID 75771—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-Chloro-benzoic acid N'-(4-amino-3-nitro-benzoyl)-hydrazideHCID 46651557—

Reaction Steps

To 4-Chloro-benzoic acid hydrazide (5.0 g, 29 mmol) and 4-Amino-3-nitro-benzoic acid (5.3 g, 29 mmol) in DMF (100 mL) was added HOBT (3.9 g, 29 mmol), and EDCI (5.5 g, 29 mmol), followed by triethylamine (12.1 mL, 87 mmol). The mixture was stirred at ambient temperature for 18 hours. Water (50 mL) was added to the reaction mixture. The precipitate was collected by filtration, washed with water, and dried under vacuum to provide the title compound as a yellow solid. 1H NMR(DMSO-d6, 400MHz) δ ppm 7.08 (d, J=8.97 Hz, 1 H) 7.61 (m, 2 H) 7.82-7.97 (m, 5 H) 8.66 (d,J=2.15 Hz, 1 H) 10.52 (s, 1 H) 10.57 (s, 1 H; (M+H)+=335.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217065B2
Source datasetuspto-grants-2012_07
ORD IDord-9af772b74cf94eb085716ca95e56aeea
Source noteuspto-grants-2012_07