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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642333Generated: October 31, 2026

2-Nitrobenzoyl chloride → 3-(2-Nitro-benzoylamino)-furo[3,2-c]pyrazole-1,5-dicarboxylic acid 1-ethyl ester 5-propyl ester

https://huagongshe.com/reaction/1642333

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Nitrobenzoyl chlorideHCID 11875—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Amino-furo[3,2-c]pyrazole-1,5-dicarboxylic acid 1-ethyl ester 5-propyl esterHCID 42601725—
SolventTetrahydrofuranHCID 8028—
Product3-(2-Nitro-benzoylamino)-furo[3,2-c]pyrazole-1,5-dicarboxylic acid 1-ethyl ester 5-propyl esterHCID 5787864974.1%

Reaction Steps

To a solution of 3-amino-furo[3,2-c]pyrazole-1,5-dicarboxylic acid 1-ethyl ester 5-propyl ester (500 mg, 1.606 mmol) and diisopropylethylamine (DIEA, 0.824 mL, 4.818 mmol) in tetrahydrofuran (THF, 20 mL) at 0° C., 2-nitro-benzoyl chloride (0.318 mL, 2.409 mmol) was added. The reaction mixture was kept at the same temperature for 10 minutes then allowed to reach room temperature and let react overnight. The solvent was removed under vacuum, the residue was dissolved in dichloromethane (DCM) and washed with a 10% solution of acetic acid (AcOH), water, saturated NaHCO3 and brine. The crude was purified on silica gel (eluant dichloromethane/methanol 96/4) yielding 512 mg (69%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119641B2
Source datasetuspto-grants-2012_02
ORD IDord-f46b149c0e424338a2a73f391a7309dc
Source noteuspto-grants-2012_02