反応 #156920

反応方程式

N,N-diisopropylethylamine

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

3-fluoro-N-isopropyl-4-(piperazin-1-yl)benzamide hydrochloride

(cyanomethyl)trimethylphosphonium iodide

→

(S)-3-fluoro-N-isopropyl-4-(4-((6-oxo-5,6,6a,7,8,9-hexahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-3-yl)methyl)piperazin-1-yl)benzamide

収率 33.6%

溶媒

propiononitrile

反応条件

後処理

1. 1
   温度It was cooled to room temperature
2. 2
   濃縮concentrated in vacuo
3. 3
   workup.DISSOLUTIONdissolved in DMSO (2 mL)
4. 4
   その他purified
5. 5
   濃縮The fractions were concentrated in vacuo
6. 6
   その他the resulting solid was recrystallized from water-MeOH (2:1, 6 mL)
7. 7
   その他dried in vacuum

実験手順

(S)-3-(hydroxymethyl)-6a,7,8,9-tetrahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-6(5H)-one (100 mg, 0.456 mmol), 3-fluoro-N-isopropyl-4-(piperazin-1-yl)benzamide hydrochloride (138 mg, 0.456 mmol), (cyanomethyl)trimethylphosphonium iodide (166 mg, 0.684 mmol) and N,N-diisopropylethylamine (0.398 ml, 2.281 mmol) were suspended in propiononitrile (Volume: 1.370 ml) and heated in a closed vial at 90-120° C. for 4 h. The reaction mixture became a dark brown solution. It was cooled to room temperature, concentrated in vacuo, dissolved in DMSO (2 mL) and purified using HPLC (basic, 45-95% ACN in water, basic). The fractions were concentrated in vacuo and the resulting solid was recrystallized from water-MeOH (2:1, 6 mL) and dried in vacuum to afford (S)-3-fluoro-N-isopropyl-4-(4-((6-oxo-5,6,6a,7,8,9-hexahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-3-yl)methyl)piperazin-1-yl)benzamide (71.4 mg, 0.153 mmol, 33.6% yield) as a light yellow solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.14 (d, J=6.57 Hz, 6 H) 1.82-2.01 (m, 3 H) 2.12-2.24 (m, 1 H) 2.46-2.50 (m, 4 H) 2.98-3.15 (m, 4 H) 3.35-3.44 (m, 3 H) 3.54-3.64 (m, 1 H) 3.92-4.14 (m, 2 H) 6.98 (d, J=1.77 Hz, 1 H) 7.03 (t, J=8.84 Hz, 1 H) 7.56-7.66 (m, 3 H) 8.09 (d, J=7.83 Hz, 1 H) 10.45 (s, 1 H). [M+H] calc'd for C25H31FN6O2, 467; found, 467.

出典