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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 549429Erstellt: 26. Oktober 2026

2-Nitrobenzoyl chloride → 3-(2-Nitro-benzoylamino)-thieno[2,3-c]pyrazole-1,5-dicarboxylic Acid 5-tert-butyl Ester 1-ethyl Ester

https://huagongshe.com/reaction/549429

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Nitrobenzoyl chlorideHCID 11875—
EduktDiisopropylethylamineHCID 81531—
Edukt5-tert-butyl 1-ethyl 3-amino-1H-thieno[2,3-c]pyrazole-1,5-dicarboxylateHCID 57737272—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(2-Nitro-benzoylamino)-thieno[2,3-c]pyrazole-1,5-dicarboxylic Acid 5-tert-butyl Ester 1-ethyl EsterHCID 5773726569,2%

Reaktionsschritte

To a solution of 5-tert-butyl 1-ethyl 3-amino-1H-thieno[2,3-c]pyrazole-1,5-dicarboxylate (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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07943654B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-3a9d4cf274c4427fa0a0dc9f7027a263
Quellennotizuspto-grants-2011_05