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

HRID 2097805ノート

反応式

HRID 2097805 の反応式
Cl.[C:2]1([N:8]2[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[I-].C(C[P+](C)(C)C)#N.O[CH2:23][C:24]1[CH:33]=[N:32][C:31]2[N:30]3[CH2:34][CH2:35][CH2:36][C@H:29]3[C:28](=[O:37])[NH:27][C:26]=2[CH:25]=1.CCN(C(C)C)C(C)C>C(#N)CC>[C:2]1([N:8]2[CH2:13][CH2:12][N:11]([CH2:23][C:24]3[CH:33]=[N:32][C:31]4[N:30]5[CH2:34][CH2:35][CH2:36][C@H:29]5[C:28](=[O:37])[NH:27][C:26]=4[CH:25]=3)[CH2:10][CH2:9]2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

6

反応条件

温度
90 °C

実験手順

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.

後処理

  1. washThe reaction mixture was washed with water (1 mL)
  2. concentrationconcentrated
  3. dissolutionThe residue was dissolved in DMSO (1 mL)
  4. custompurified
  5. concentrationThe fractions were concentrated in vacuo
  6. dissolutiondissolved in dioxane-water (1:1, 2 mL)

出典と根拠

ORDレコード
ord-de9cabcaa9a7439b9772c69bec2891a5
出典データセット
uspto-grants-2013_05
特許番号
US08450323B2

反応ノート

読み込み中…