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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095412Generated: October 30, 2026

Ether hydrochloride → 3-[4-(2-Phenoxyethyl)-1-piperidinyl]-5-[(2(S)-pyrrolidinyl)methoxy]pyridine Hydrochloride

https://huagongshe.com/reaction/2095412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEther hydrochlorideHCID 10953452—
Reactant3-[[1-(tert-Butoxycarbonyl)-2(S)-pyrrolidinyl]methoxy]-5-[4-(2-phenoxyethyl)-1-piperidinyl]pyridineHCID 59371675—
SolventMethanolHCID 887—
Product3-[4-(2-Phenoxyethyl)-1-piperidinyl]-5-[(2(S)-pyrrolidinyl)methoxy]pyridine HydrochlorideHCID 68612871—

Reaction Steps

To a solution of 3-[[1-(tert-butoxycarbonyl)-2(S)-pyrrolidinyl]methoxy]-5-[4-(2-phenoxyethyl)-1-piperidinyl]pyridine (150 mg, 0.31 mmol) in MeOH (0.5 mL) was added 2N anhydrous HCl/ether (2 mL) under Ar at room temperature. The mixture was stirred at room temperature overnight. After the solvent was evaporated, the residue was dissolved in deionized water. The aqueous solution was washed twice with EtOAc, then filtered over a cotton plug. The water was removed under reduced pressure at 35° C., and the residue was purified by HPLC (ACE AQ 150×21.2 mm; UV detection at 254 and 280 nm; flow 10.0 mL/min; gradient of 0 to 50% CH3CN in water [both containing 0.05 vol % CF3COOH] in 25 min, to 100% in another 5 min; tR 13.6-19.7 min) to obtain, after evaporation, the trifluoroacetate (131 mg). This salt was treated with PL-HCO3 MP anion exchange resin (Polymer Laboratories) in MeOH. to afford the free amine. The solution was evaporated, and the residue was dissolved in MeOH (0.5 mL) and treated again with 2N anhydrous HCl/ether (2 mL) under Ar protection at room temperature. The mixture was stirred at room temperature overnight. After the solvent was evaporated, the residue was dissolved in deionized water. The solution was filtered over a cotton plug, and the water was removed under reduced pressure at 35° C. After lyophilization from water, the hydrochloride (117 mg) was obtained as a colorless solid. [α]20D+2.6 (c 6.9 g/L, MeOH). 1H NMR (D2O, 400 MHz) δ 7.59 (s, 1H), 7.13 (s, 1H), 6.92 (m, 2H), 6.57 (m, 3H), 4.22 (m, 1H), 4.08 (m, 1H), 3.88 (m, 1H), 3.60 (m, 2H), 3.41 (m, 2H), 3.18 (m, 2H, J=6.8 Hz), 2.52 (m, 2H), 2.04-2.00 (m, 1H), 2.00-1.80 (m, 2H), 1.78-1.62 (m, 1H), 1.43 (m, 2H), 1.31 (m, 3H), 0.93 (m, 2H). 13C NMR (D2O, 100 MHz) δ 157.9, 156.4, 148.5, 129.1, 121.2, 120.4, 117.2, 114.0, 67.3, 65.2, 58.0, 47.0, 45.5, 34.4, 31.1, 30.1, 25.4, 23.0. HRMS (ESI) calcd for C23H32N3O2 (M+H+) m/z 382.2495, found 382.2484. Anal. Calcd. for C23H31N3O2.2.2HCl.0.7H2O: C, 58.24; H, 7.35; N, 8.86; Cl, 16.44. Found: C, 58.36; H, 7.33; N, 8.80; Cl, 16.12.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445684B2
Source datasetuspto-grants-2013_05
ORD IDord-aa7fd02643044243bff911712ab77692
Source noteuspto-grants-2013_05