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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929137Generated: October 31, 2026

Imidazole → 4-(5-Amino-6-nitro-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/929137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
Reactant5-Amino-6-nitro-1H-isoindole-1,3(2H)-dioneHCID 15144568—
Solvent1,4-DioxaneHCID 31275—
Product4-(5-Amino-6-nitro-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-piperidine-1-carboxylic acid tert-butyl esterHCID 6679365554%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 5-amino-6-nitro-isoindole-1,3-dione (2.07 g, 10 mmol), tert-butyl 4-amino-piperidine-1-carboxylate (2.5 g, 12 mmol), imidazole (1.63 g, 24 mmol) in dioxane (100 mL) was sealed in a ChemGlass heavy wall pressure flask. After it was heated at 140° C. for 72 h, the reaction mixture was evaporated to dryness at 95° C. (the bath temperature) under reduced pressure. The chromatography of the residue with CH2Cl2/MeOH/28% aqueous NH4OH (320:10:1) afforded the title compound (2.09 g, 54%). 1H NMR (CDCl3) δ 1.49 (s, 9H), 1.73 (m, 2H), 2.38 (m, 2H), 2.80 (m, 2H), 4.20-4.31 (3H), 7.03 (br s, 2H, NH), 7.34 (s, 1H), 8.61 (s, 1H); ESI-MS m/z 391.5 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290503B2
Source datasetuspto-grants-2016_03
ORD IDord-58244baf382646e890a28c35a59b020a
Source noteuspto-grants-2016_03