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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230472Generated: October 30, 2026

HCID 2974347, compound → HCID 57438148, compound

https://huagongshe.com/reaction/230472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 2974347HCID 2974347—
ReactantHCID 22272508HCID 22272508—
CatalystNickelHCID 935—
ProductHCID 57438148HCID 5743814890%

Reaction Steps

N-Ethyl-5-(4-methyl-1-piperazinyl)-2-nitroaniline was reduced with Raney-Ni as described previously for the synthesis of tert-butyl 4-[4-amino-3-(ethylamino)phenyl]-1-piperazinecarboxylate to give N-2-ethyl-4-(4-methyl-1-piperazinyl)-1,2-benzenediamine (yield >90%) as a red oil. The product is very sensitive to oxidation and was therefore used immediately in the next reaction step. HPLC purity >90%; MS (posEI) m/z=234 (M+);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566715B2
Source datasetuspto-grants-2009_07
ORD IDord-306c4832b03a4988b374dada039fd3cb
Source noteuspto-grants-2009_07