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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690425Generated: November 2, 2026

3-Aminopiperidine-2,6-dione hydrochloride → HCID 24938453, compound

https://huagongshe.com/reaction/1690425

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Aminopiperidine-2,6-dione hydrochlorideHCID 134548—
ReactantHCID 66906664HCID 66906664—
SolventPyridineHCID 1049—
ProductHCID 24938453HCID 2493845388%

Reaction Steps

A mixture of 3-(2-methoxy-phenoxy)-phthalic acid (0.51 g, 1.8 mmol) and rac-α-aminoglutarimide hydrochloride (0.29 g, 1.8 mmol) in pyridine (10 mL) was heated to reflux for 16 h. The mixture was cooled and evaporated under vacuum. The residue was dissolved in ethyl acetate (100 mL) and washed with dilute aqueous HCl (2×100 mL) and water (100 mL), and was evaporated. The residue was chromatographed using a CH2Cl2-methanol gradient, eluting the title compound at 95:5 CH2Cl2-methanol, 0.59 g, in 88% yield; mp 223-225° C.; HPLC, Waters Symmetry C-18, 3.9×150 mm, 5 μm, 1 mL/min, 240 nm, 40/60 CH3CN/0.1% H3PO4, 6.06 (99.46%); 1H NMR (DMSO-d6) δ 2.06-2.11 (m, 1H), 2.53-2.64 (m, 2H), 2.83-2.90 (m, 1H), 3.75 (s, 1H), 5.15 (dd, J=12.4 Hz, J=5.3 Hz, 1H), 6.85 (d, J=8.5 Hz, 1H), 7.06 (t, J=7.3 Hz, 1H), 7.21-7.37 (m, 3H), 7.54 (d, J=7.2 Hz, 1H), 7.72 (t, J=7.9 Hz, 1H), 11.13 (s, 1H); 13C NMR (DMSO-d6) δ 21.9, 31.0, 48.9, 55.7, 113.7, 116.5, 116.7, 120.7, 121.5, 122.3, 127.2, 133.3, 137.0, 141.3, 151.2, 154.7, 165.0, 166.6, 170.0, 172.8; Anal. Calcd for C20H16N2O6: C, 63.16; H, 4.24; N, 7.37. Found: C, 63.00; H, 4.24; N, 7.29.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153659B2
Source datasetuspto-grants-2012_04
ORD IDord-4bd4c40e028c4970abe58ea538f0ee34
Source noteuspto-grants-2012_04