Diethyl Ether → 6-[N-(5-bromo-2-hydroxybenzyl)-N-ethylamino]-pyridazine-3-carboxamide
反応式
C([O:8][C:9]1[CH:27]=[CH:26][C:25]([Br:28])=[CH:24][C:10]=1[CH2:11][N:12]([C:15]1[N:20]=[N:19][C:18]([C:21]([NH2:23])=[O:22])=[CH:17][CH:16]=1)[CH2:13][CH3:14])C1C=CC=CC=1.CSC.B(Cl)(Cl)Cl.C(=O)(O)[O-].[Na+].C(OCC)C>ClCCl.CO>[Br:28][C:25]1[CH:26]=[CH:27][C:9]([OH:8])=[C:10]([CH:24]=1)[CH2:11][N:12]([C:15]1[N:20]=[N:19][C:18]([C:21]([NH2:23])=[O:22])=[CH:17][CH:16]=1)[CH2:13][CH3:14]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
6-[N-(2-Benzyloxy-5-bromobenzyl)-N-ethylamino]pyridazine-3-carboxamide (3.24 g, 7.3 mmol) in dichloromethane (50 ml) was treated with boron trichloride dimethyl sulphide reagent (18.5 ml, 2M solution) in dichloromethane (37 mmol) and the solution stirred at ambient temperature for 6 days. The mixture was carefully treated with excess aqueous sodium bicarbonate solution to give a pH of around 9. Dichloromethane was added, the organic and aqueous layers separated and the aqueous layer washed with dichloromethane. The combined organic extracts were then washed with brine, dried and evaporated to give a sticky solid. This was treated with diethylether (30 ml) and methanol (3 ml) and left at ambient temperature overnight. The resultant solid was filtered, washed with diethylether and sucked dry to give 6-[N-(5-bromo-2-hydroxybenzyl)-N-ethylamino]-pyridazine-3-carboxamide (1.34 g, 52%).
後処理
- customto give a pH of around 9
- customthe organic and aqueous layers separated
- washthe aqueous layer washed with dichloromethane
- washThe combined organic extracts were then washed with brine
- customdried
- customevaporated
- customto give a sticky solid
- waitleft at ambient temperature overnight
- filtrationThe resultant solid was filtered
- washwashed with diethylether
- customsucked dry
出典と根拠
- ORDレコード
- ord-cb7e2cfed299473985791b6c1cc2edde
- 出典データセット
- uspto-grants-2000_08
- 特許番号
- US06100258
反応ノート
読み込み中…