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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448416Generated: October 30, 2026

3-Amino-3-methylpiperidine-2,6-dione hydrochloride → HCID 67230396, compound

https://huagongshe.com/reaction/448416

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-3-methylpiperidine-2,6-dione hydrochlorideHCID 21928252—
ReactantHCID 67230375HCID 67230375—
SolventPyridineHCID 1049—
ProductHCID 67230396HCID 6723039651.2%

Reaction Steps

A mixture of 3-(t-butoxycarbonylamino-methyl)-phthalic acid (3.3 g, 11.2 mmol) and 3-amino-3-methyl-piperidine-2,6-dione hydrochloride (2.0 g, 11.2 mmol) in pyridine (40 mL) was refluxed for 17 hours. The mixture was cooled and concentrated. The residue was dissolved in EtOAc (200 mL) and water (50 mL). The organic layer was washed with water (40 mL), Sat. NaHCO3 (40 mL), water (40 mL), and brine (40 mL), and dried (MgSO4). Solvent was removed, and the residue was purified by chromatography (Silica gel) to give [2-(3-methyl-2,6-dioxo-piperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-isoindol-4-ylmethyl]-carbamic acid t-butyl ester (2.3 g, 51%): 1H NMR (CDCl3) δ 1.43 (s, 9H, 3(CH3)), 2.08 (s, 3H, CH3), 2.10-2.15 (m, 1H), 2.69-2.84 (m, 3H), 4.62 (d, J=6.5 Hz, 2H, CH2), 5.46 (m, 1H, NH), 7.64-7.76 (m, 3H, Ar), 8.15 (s, 1H, NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481568B2
Source datasetuspto-grants-2013_07
ORD IDord-d63464dd3e5c4446a4a87557b0ed7742
Source noteuspto-grants-2013_07