تفاعل #2182594

معادلة التفاعل

3-[[1-(tert-butoxycarbonyl)-2(S)-pyrrolidinyl]methoxy]-5-[4-(2-phenoxyethyl)-1-piperidinyl]pyridine

HCl ether

→

amine

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

المذيبات

MeOH

ظروف التفاعل

المعالجة

1. 1
   أخرىAfter the solvent was evaporated
2. 2
   workup.DISSOLUTIONthe residue was dissolved in deionized water
3. 3
   غسيلThe aqueous solution was washed twice with EtOAc
4. 4
   ترشيحfiltered over a cotton plug
5. 5
   أخرىThe water was removed under reduced pressure at 35° C.
6. 6
   أخرىthe residue was purified by HPLC (ACE AQ 150×21.2 mm
7. 7
   workup.WAITgradient of 0 to 50% CH3CN in water [both containing 0.05 vol % CF3COOH] in 25 min
8. 8
   workup.WAITto 100% in another 5 min
9. 9
   أخرىtR 13.6-19.7 min) to obtain
10. 10
    أخرىafter evaporation
11. 11
    workup.ADDITIONThis salt was treated with PL-HCO3 MP anion exchange resin (Polymer Laboratories) in MeOH

الإجراء التجريبي

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.

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