反応 #1121781

ord-c64fe8931435479e8b0e4572e241bf33

反応方程式

COc1ccc(Sc2[nH]c(-c3ccccc3)cn3c(=O)c(Cc4ccccc4)nc2-3)cc1
231
COc1ccc(Sc2[nH]c(-c3ccccc3)cn3c(=O)c(Cc4ccccc4)nc2-3)cc1
2-Benzyl-8-(4-methoxyphenylthio)-6-phenylimidazo[1,2-a]pyrazin-3(7H)-one
CC(=O)Cl
acetyl chloride
COc1ccc(Sc2nc(-c3ccccc3)cn3c(OC(C)=O)c(Cc4ccccc4)nc23)cc1
25a
収率 66.0%
COc1ccc(Sc2nc(-c3ccccc3)cn3c(OC(C)=O)c(Cc4ccccc4)nc23)cc1
2-Benzyl-8-(4-methoxyphenylthio)-6-phenylimidazo[1,2-a]pyrazin-3-yl acetate
収率 66.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    洗浄Then the solution was washed with water
  2. 2
    乾燥the organic layer was dried over Na2SO4
  3. 3
    ろ過filtered
  4. 4
    その他the solvent removed under reduced pressure

実験手順

To a solution of 231 (25 mg, 0.06 mmol) in 4 mL of dichloromethane, acetyl chloride (8 μL, 0.12 mmol) and 4-(dimethylamino)pyridine (DMAP) (5 mg, 0.03 mmol) were added, the resulting mixture was stirred at room temperature for 15 min. Then the solution was washed with water and the organic layer was dried over Na2SO4, filtered and the solvent removed under reduced pressure to obtain 18 mg (yield 66%) of 25a as a red oil. 1H-NMR (CDCl3): 2.10 (s, 3H), 3.88 (s, 3H), 4.20 (s, 2H), 7.00-7.02 (m, 2H), 7.22-7.33 (m, 8H), 7.61-7.64 (m, 4H), 7.68 (s, 1H). MS (ESI): m/z 482 (M+H+).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08546147B2uspto-grants-2013_10