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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428431Generated: October 31, 2026

Ethyl 4-(4-chloro-2-nitrobenzoyl)-3-benzoyl-1H-pyrazole-5-carboxylate → ethyl 4-(4-chloro-2-aminobenzoyl)-3-benzoyl-1H-pyrazole-5-carboxylate

https://huagongshe.com/reaction/428431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-(4-chloro-2-nitrobenzoyl)-3-benzoyl-1H-pyrazole-5-carboxylateHCID 18358884—
Catalystnickel boride (NiB)HCID 82791—
Productethyl 4-(4-chloro-2-aminobenzoyl)-3-benzoyl-1H-pyrazole-5-carboxylateHCID 1835887256%

Reaction Steps

Following a procedure similar to that described in Example 23(d), ethyl 4-(4-chloro-2-nitrobenzoyl)-3-benzoyl-1H-pyrazole-5-carboxylate (1.2 g, 2.81 mmol) was treated with nickel boride to afford crude product. The crude product was purified by flash chromatography eluting with hexanes:ethyl acetate (75:25-50:50) to give the title compound as a solid (620 mg, 56%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313290B1
Source datasetuspto-grants-2001_11
ORD IDord-acd8336ef3464b86830d341a31fb2911
Source noteuspto-grants-2001_11