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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216463Generated: October 31, 2026

Hydrochloric Acid → HCID 21896937, compound

https://huagongshe.com/reaction/2216463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant1-Methyl-4-(methylamino)piperidineHCID 566323—
ReactantHCID 21897131HCID 21897131—
SolventAcetoneHCID 180—
Solvent1,4-DioxaneHCID 31275—
ProductAmmonium HydroxideHCID 14923—
ProductHCID 21896937HCID 2189693717.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a sample of 102 (0.286 g, 1.0 mmol) dissolved in 1,4-dioxane (4 mL) was added a solution of N-methyl-4(methylamino)piperidine (0.15 mL, 1.0 mmol) in acetone (1 mL) followed by addition of a NaOH solution (0.0462 g, 1.0 mmol dissolved in 1 mL of H2O). The reaction mixture was allowed to stir at about 80° C. for about 2 hours. The reaction mixture was poured over crushed ice and neutralized with 10% HCl (aq). The resulting solid was collected by vacuum filtration, washed with water and dried under vacuum overnight. Column chromatography (silica gel, 96:3:1 dichloromethane:methanol:conc. ammonium hydroxide) yielded a light purple solid 103 (41 mg, 9%), mp 84° C.; HPLC: YMC Pack Pro C18, 40:30:30 [KH2PO4 (0.01M, pH 3.2): CH3OH: CH3CN], 264 nm, Rt 12.7 min, 97% purity); 1H NMR (600 MHz, CDCl3, 55° C.) δ 7.98 (s, 1H), 7.18 (S, 1H), 6.85 (d, J=9 Hz, 1H), 6.58 (s, 1H), 4.89 (s, 1H), 4.58-4.62 (m, 1H), 3.87 (s, 3H), 3.25 (t, J=6.6 Hz, 2H), 3.05 (s, 3H), 2.94 (d, J=11.4 Hz, 2H), 2.31 (s, 3H), 2.15 (S, 2H), 1.86 (dq, J=12,4.2 Hz, 3H), 1.57-1.78 (m, 8H), 1.15-1.30 (m, 4H), 1.00 (dq, J=11.4, 3 Hz, 2H); MS (ESI): m/z 476 (37.7), 474 (M+H, 100), 410 (1.4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112587B2
Source datasetuspto-grants-2006_09
ORD IDord-a7bedded1d0e4e858a009a523877f96a
Source noteuspto-grants-2006_09