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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987762Generated: October 26, 2026

1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → (+/-)-(5-Nitro-2,4,6,7-tetramethyldihydrobenzofuran-2-yl)-[4-(4-1h-pyrazol-5-ylphenyl)-piperazin-1-yl]carboxamide

https://huagongshe.com/reaction/1987762

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHOBT hydrochlorideHCID 22729017—
Reactant1-(4-1H-pyrazol-5-ylphenyl)-piperazineHCID 23118309—
Reactant2,4,6,7-Tetramethyl-5-nitrodihydrobenzofuran-2-carboxylic acidHCID 68844454—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
Product(+/-)-(5-Nitro-2,4,6,7-tetramethyldihydrobenzofuran-2-yl)-[4-(4-1h-pyrazol-5-ylphenyl)-piperazin-1-yl]carboxamideHCID 6884548090.6%

Reaction Steps

To 0.38 g of 1-(4-1H-pyrazol-5-ylphenyl)-piperazine and 0.4 g of 2,4,6,7-tetramethyl-5-nitrodihydrobenzofuran-2-carboxylic acid, 0.35 g of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, 0.25 g of 1-hydroxybenzotriazole hydrochloride and 0.19 g of triethylamine were added, followed by stirring at room temperature for 24 hours. The reaction solution was poured into water and the precipitated crystal was removed by filtration and washed with water, and then the resulting crystal was dried to obtain 0.65 g of the objective compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07553837B2
Source datasetuspto-grants-2009_06
ORD IDord-41996fa04e8343d4bc13a543273b67dc
Source noteuspto-grants-2009_06