Reacción #156786

Ecuación de reacción

DIPEA

1-Phenylpiperazine hydrochloride

(cyanomethyl)trimethylphosphonium iodide

(S)-3-(hydroxymethyl)-6a,7,8,9-tetrahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-6(5H)-one

→

title compound

Rendimiento 23.4%

(S)-3-((4-phenylpiperazin-1-yl)methyl)-6a,7,8,9-tetrahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-6(5H)-one

Rendimiento 23.4%

Disolventes

propionitrile

Condiciones de reacción

Tratamiento posterior

1. 1
   LavadoThe reaction mixture was washed with water (1 mL)
2. 2
   Concentraciónconcentrated
3. 3
   workup.DISSOLUTIONThe residue was dissolved in DMSO (1 mL)
4. 4
   Otropurified
5. 5
   ConcentraciónThe fractions were concentrated in vacuo
6. 6
   workup.DISSOLUTIONdissolved in dioxane-water (1:1:, 2 mL)

Procedimiento

1-Phenylpiperazine hydrochloride (11.9 mg, 0.060 mmol), (cyanomethyl)trimethylphosphonium iodide (0.025 g, 0.102 mmoles), and (S)-3-(hydroxymethyl)-6a,7,8,9-tetrahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-6(5H)-one (0.014 g, 0.063 mmoles) were diluted with propionitrile (0.5 ml) and treated with DIPEA (0.017 ml, 0.100 mmol). The reaction mixture was stirred at 90° C. overnight. The reaction mixture was washed with water (1 mL) and concentrated. The residue was dissolved in DMSO (1 mL) and purified using HPLC (acetonitrile-water, NH4HCO3 buffered). The fractions were concentrated in vacuo, dissolved in dioxane-water (1:1:, 2 mL) and lyophilized to yield the title compound as a white solid (5.1 mg, 23%). [M+H] calc'd for C21H25N5O 364; found, 364.

Fuente