反応 #308147

ord-19cc54e88f3e4e4b9311635b7e3cb69e

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他at room temperature
  2. 2
    洗浄washed with saturated NaHCO3
  3. 3
    乾燥brine, dried
  4. 4
    濃縮concentrated in vacuo
  5. 5
    その他The residue was purified by preparative HPLC (eluant; 0.5% 35% ammonia:9.5% methanol:90% dichloromethane)
  6. 6
    その他to give a white powder

実験手順

DIEA (0.135 ml, 0.78 mmol) and isobutyryl chloride (0.029 ml, 0.27 mmol) were added to a solution of (4-aminomethyl-3-fluoro-phenyl)-(6-chloro-3-methyl-4,10-dihydro-3H-2,3,4,9-tetraaza-benzo[f]azulen-9-yl)-methanone hydrochloride from Example E102.2 (110 mg, 0.26 mmol) in dichloromethane (3 ml) at room temperature. The mixture was stirred for 1 h, washed with saturated NaHCO3 then brine, dried and concentrated in vacuo. The residue was purified by preparative HPLC (eluant; 0.5% 35% ammonia:9.5% methanol:90% dichloromethane) to give a white powder identified as the title compound (85 mg, 71%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08202858B2uspto-grants-2012_06