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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929089Generated: October 26, 2026

1-Hydroxybenzotriazole → 5-Amino-4-methyl-2-(1-methyl-piperidin-4-yl)-6-nitro-isoindole-1,3-dione

https://huagongshe.com/reaction/929089

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Methylpiperidin-4-amine dihydrochlorideHCID 22002536—
Reactant4-Amino-2-(methoxycarbonyl)-3-methyl-5-nitrobenzoic acidHCID 59761680—
SolventTriethylamineHCID 8471—
Product5-Amino-4-methyl-2-(1-methyl-piperidin-4-yl)-6-nitro-isoindole-1,3-dioneHCID 59761859104.3%

Reaction Steps

To a solution of 4-Amino-3-methyl-5-nitro-phthalic acid 2-methyl ester (1.3 g, 5.12 mmol), EDCI.HCl (1.07 g, 5.63 mmol) and HOBt (0.69 g, 5.12 mmol) was added Et3N (3.64 mL, 25.6 mL) and stirred at room temperature for 10 min. 4-Amino-1-methylpiperidine dihydrochloride (1.04 g, 5.63 mmol) was added and the resulting mixture was stirred at room temperature for 24 h. The reaction mixture was evaporated in vacuo, the residue was dissolved in CHCl3 (200 mL), washed with water (2×100 mL). The organic layer was filtered over Na2SO4 and concentrated in vacuo to afford 5-Amino-4-methyl-2-(1-methyl-piperidin-4-yl)-6-nitro-isoindole-1,3-dione (1.7 g, quant), which was used as such for further reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290503B2
Source datasetuspto-grants-2016_03
ORD IDord-fe9cbe9afa6d4e089473d5ffa9092dac
Source noteuspto-grants-2016_03