Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646925Generated: November 1, 2026

Hydrochloric Acid → HCID 10331340, compound

https://huagongshe.com/reaction/1646925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
ReactantChloropyrazineHCID 73277—
Reactant3-Piperidinone, 1-methyl-HCID 79656—
ReactantButyllithiumHCID 178418339—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 10331340HCID 1033134053.4%

Reaction Conditions

Temperature-77 °C

Reaction Steps

A solution of 7.2 ml 2,2,6,6-tetramethylpiperidine (0.034 mol) in 300 ml of dry THF was cooled to -8° C. as 25 ml of 1.6 M butyllithium (0.04 mol) in hexane was added dropwise. The reaction was stirred 20 min then cooled to -77° C. A solution of 2.9 ml of 2-chloropyrazine (0.031 mol) in 5 ml of THF was added dropwise to the reaction. After another 15 min, 3.5 g of 1-methylpiperidin-3-one (0.035 mol) in 10 ml of THF was added dropwise. After the addition, the reaction was stirred 1.5 h followed by addition of a mixture of 8 ml of concentrated HCl and 4 ml of ethanol. The cooling was removed and when the temperature had reached -15° C., 20 ml of 5 N NaOH was added. The volatile organics were evaporated and the aqueous residue was extracted 4 × with 30 ml of CH2Cl2. The extracts were washed with brine, dried and the solvent evaporated to give a brown solid that was dissolved in 300 ml of ether and filtered. The ether was evaporated and the residue recrystallized from hexane to give 3.77 g of (1), 53% yield, mp 111°-112° C. NMR ppm (CDCl3) 1.7-2.2 (5H,m), 2.4 (3H, s), 2.7 (1H, d), 2.85-3.05 (2H, m), 4.4 (1H, bs), 8.35 (1H, d), 8.5 (1H, d). Anal. C10H14ClN3O, requires C: 52.75; H: 6.20; N: 18.46%. Found C: 52.64; H: 6.21; N: 18.21%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05182283
Source datasetuspto-grants-1993_01
ORD IDord-b683ee1a6c85459d9625a924db28ac8b
Source noteuspto-grants-1993_01