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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709537Generated: October 29, 2026

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

https://huagongshe.com/reaction/709537

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 HO (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 numberUS09181216B2
Source datasetuspto-grants-2015_11
ORD IDord-13ea5d4c24d04d829d2e0b995c175c47
Source noteuspto-grants-2015_11