Dimethylformamide → Methyl 5-(thiazol-4-ylmethoxy)pyrazine-2-carboxylate

HRID 1526597ノート

反応式

HRID 1526597 の反応式
Cl[C:2]1[N:3]=[CH:4][C:5]([C:8]([O:10][CH3:11])=[O:9])=[N:6][CH:7]=1.[S:12]1[CH:16]=[C:15]([CH2:17][OH:18])[N:14]=[CH:13]1.C(=O)([O-])[O-].[Cs+].[Cs+].CN(C=O)C>O>[S:12]1[CH:16]=[C:15]([CH2:17][O:18][C:2]2[N:3]=[CH:4][C:5]([C:8]([O:10][CH3:11])=[O:9])=[N:6][CH:7]=2)[N:14]=[CH:13]1

参加物

6

反応条件

温度
40 °C

実験手順

A RBF was charged with methyl 5-chloropyrazine-2-carboxylate (1.239 g, 7.18 mmol, Ark Pharm), thiazol-4-ylmethanol (0.8266 g, 7.18 mmol), cesium carbonate (0.689 ml, 8.61 mmol, Alfa Aesar) and DMF (20.51 ml). The reaction mixture was stirred at 40° C. for 3 days. The reaction mixture was allowed to cool to rt and was diluted with water and extracted with EtOAc. The organic extract was washed with water, satd NaCl, dried over MgSO4, and concentrated in vacuo. The crude product was adsorbed onto a plug of silica gel and purified by silica gel flash chromatography, eluting with a gradient of 10% to 100% EtOAc in hexane, to provide methyl 5-(thiazol-4-ylmethoxy)pyrazine-2-carboxylate (0.7606 g, 3.03 mmol, 42.2% yield). MS m/z=252.1 [M+H]+. Calculated for C10H9N3O3S: 251.036. 1H NMR (400 MHz, DMSO-d6) δ ppm 3.89 (s, 2H) 5.60 (s, 1H) 7.86 (d, J=1.96 Hz, 1H) 8.46 (d, J=1.37 Hz, 1H) 8.86 (d, J=1.37 Hz, 1H) 9.14 (d, J=1.96 Hz, 1H)

後処理

  1. temperatureto cool to rt
  2. extractionextracted with EtOAc
  3. extractionThe organic extract
  4. washwas washed with water
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated in vacuo
  7. custompurified by silica gel flash chromatography
  8. washeluting with a gradient of 10% to 100% EtOAc in hexane

出典と根拠

ORDレコード
ord-c0801f5801694ff6a152d83ac632dbb4
出典データセット
uspto-grants-2015_07
特許番号
US09085576B2

反応ノート

読み込み中…