反応 #215835
ord-49200922f7c94b7b8d05ad8d2df8cf6e
反応方程式
3-[(2-furanylmethyl)thio]propanoic acid, hydrazide
8-chlorodibenz[b,f]oxazepine-10(11H)-carboxylic acid, 2-[1-oxo-3-(2-pyridinyl)propyl]hydrazide
8-chlorodibenz[b,f][1,41oxazepine-10(11H)-carboxylic acid, 2-[1-oxo-3-(2-pyridinyl)propyl]hydrazide
8-chlorodibenz[b,f][1,4]-oxazepine-10(11H)-carbonyl chloride
8-chlorodibenz[b,f][1,4]-oxazepine-10(11H)carbonyl chloride
→
反応物
3-[(2-furanylmethyl)thio]propanoic acid, hydrazide
8-chlorodibenz[b,f]oxazepine-10(11H)-carboxylic acid, 2-[1-oxo-3-(2-pyridinyl)propyl]hydrazide
8-chlorodibenz[b,f][1,41oxazepine-10(11H)-carboxylic acid, 2-[1-oxo-3-(2-pyridinyl)propyl]hydrazide
8-chlorodibenz[b,f][1,4]-oxazepine-10(11H)-carbonyl chloride
8-chlorodibenz[b,f][1,4]-oxazepine-10(11H)carbonyl chloride
試薬
なし
反応条件
詳細条件
See reaction.notes.procedure_details.
後処理
- 1その他was prepared
- 2その他prepared
- 3その他prepared
実験手順
8-chlorodibenz[b,f][1,41oxazepine-10(11H)-carboxylic acid, 2-[3-[(2-furanylmethyl)thio]-1-oxopropyl]hydrazide (13) was prepared in the manner 8-chlorodibenz[b,f]oxazepine-10(11H)-carboxylic acid, 2-[1-oxo-3-(2-pyridinyl)propyl]hydrazide (6) was prepared, as described above in Example 6, from 3-[(2-furanylmethyl)thio]propanoic acid, hydrazide (12), prepared as described above in Example 12, and 8-chlorodibenz[b,f][1,4]-oxazepine-10(11H)-carbonyl chloride (2), prepared as described above in Example 2, on a 10 mmol scale. The yield was quantitative. Analysis calculated for C22H20N3O4SCl (M.W. 457.94): C, 57.70; H, 4.40; N, 9.18; Cl, 7.74; S, 7.00. Found: C, 57.59; H, 4.36; N, 9.01; Cl, 7.95; S, 7.07.