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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036668Generated: October 29, 2026

3-Amino-2,6-piperidinedione → 1-Aminopiperidine-2,6-dione

https://huagongshe.com/reaction/1036668

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-2,6-piperidinedioneHCID 134508—
Reactant2-Acetoxy-n-(2,6-dioxopiperidin-3-yl)benzamideHCID 11483136—
Reactant4,7,7-Trimethyl-3-bicyclo[2.2.1]heptanecarbonyl chlorideHCID 53442783—
SolventChloroformHCID 6212—
Product1-Aminopiperidine-2,6-dioneHCID 1998213460%

Reaction Steps

A mixture of (+)-camphanic chloride (19 mg, 00868 mmol), aminoglutarimide (21 mg, 0.0868 mmol) and Et3N (24) in CHCl3 (1 ml) was stirred at room temperature for 16 hours. The solution was diluted with CHCl3, washed with saturated aqueous solution of NaHCO3, dried over Na2SO4, concentrated and purified by chromatography (silica gel, CH2Cl2; EtOAc=10:1) to give product (16 mg, 60.0% yield) as a colorless gel: 13CNMR (CDCl3) δ 172.6, 169.4, 168.6, 165.5, 90.3, 58.3, 53.3, 48.2, 47.6, 29.2, 28.2, 26.9, 22.7, 14.6, 7.6; MS (CI/CH4) m/z 308 (M+). This compound exhibited angiogenic activity in the assay of Example 13.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546430B2
Source datasetuspto-grants-2013_10
ORD IDord-a92f053e10fd4511bcb0f3206f072ba6
Source noteuspto-grants-2013_10