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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009092Generated: November 1, 2026

Triethylamine → 1-Aminopiperidine-2,6-dione

https://huagongshe.com/reaction/1009092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Amino-2,6-piperidinedioneHCID 134508—
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 μl) 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 numberUS07973057B2
Source datasetuspto-grants-2011_07
ORD IDord-b5afcbf4fdde441185a6927be3b9775f
Source noteuspto-grants-2011_07