反応 #1810685
ord-8d2e4fa9f3b24b82b383c59c2e02b557
反応方程式
反応条件
詳細条件
See reaction.notes.procedure_details.
後処理
- 1その他The title compound was prepared
実験手順
The title compound was prepared as described in Example 1 starting with (A) of Example 1 (2.0 g, 6.4 mmol) and using N-methylpiperazine in place of dibutylamine to produce 0.56 g (25% yield of the free base of the title compound which was converted to the HCl salt, mp 250°-252° C. IR: 1600 cm-1. MS: 378(MH+). 1H NMR (CDCl3): δ 7.82-7.00 (m, 10H), 4.13 (t, J=5.2 Hz, 2H), 3.31 (m, 13H), 2.41 (m, 2H).