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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262038Generated: November 2, 2026

1-(4-Nitrophenyl)piperidine-3-carboxylic acid → (4-Methyl-piperazin-1-yl)-[1-(4-nitro-phenyl)-piperidin-3-yl]-methanone

https://huagongshe.com/reaction/1262038

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Nitrophenyl)piperidine-3-carboxylic acidHCID 16769484—
Reactant(4-Methyl-piperazin-1-yl)-[1-(4-nitro-phenyl)-piperidin-3-yl]-methanoneHCID 66711465—
SolventWaterHCID 962—
Product(4-Methyl-piperazin-1-yl)-[1-(4-nitro-phenyl)-piperidin-3-yl]-methanoneHCID 66711465—
Product(4-Methyl-piperazin-1-yl)-[1-(4-nitro-phenyl)-piperidin-4-yl]-methanoneHCID 66712189—

Reaction Steps

(4-Methyl-piperazin-1-yl)-[1-(4-nitro-phenyl)-piperidin-4-yl]-methanone was prepared in a similar manner as (4-Methyl-piperazin-1-yl)-[1-(4-nitro-phenyl)-piperidin-3-yl]-methanone of Example 443a after substituting 1-(4-Nitro-phenyl)-piperidine-4-carboxylic acid for 1-(4-Nitro-phenyl)-piperidine-3-carboxylic acid. (4-Methyl-piperazin-1-yl)-[1-(4-nitro-phenyl)-piperidin-3-yl]-methanone was isolated as a yellow solid from water (570 mg, 86%). LC: 100%; LC/MS (E/I+) 333.13 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08471005B2
Source datasetuspto-grants-2013_06
ORD IDord-5cb5a833d1e449539e7efdef3fc28254
Source noteuspto-grants-2013_06