Sulfuric Acid → 7-Hydroxy-1,2,4,5-tetrahydro-benzo[d]azepine-3-carboxylic acid ethyl ester
反応式
N[C:2]1[CH:17]=[CH:16][C:5]2[CH2:6][CH2:7][N:8]([C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH2:9][CH2:10][C:4]=2[CH:3]=1.S(=O)(=O)(O)[OH:19]>N([O-])=O.[Na+]>[OH:19][C:2]1[CH:17]=[CH:16][C:5]2[CH2:6][CH2:7][N:8]([C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH2:9][CH2:10][C:4]=2[CH:3]=1参加物
実験手順
To ethyl 7-amino-1,2,4,5-tetrahydro-3H-3-benzazepine-3-carboxylate was added a 5% aqueous sulfuric acid solution, followed by stirring under ice-cooling. An aqueous solution (30 ml) of 10.22 g of sodium nitrite was added dropwise in portions thereto, and followed by stirring at the same temperature for 0.5 hours and then stirring at 60° C. for 3 hours. The reaction mixture was extracted with ethyl acetate, the organic layer was dried over anhydrous magnesium sulfate and then filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel chromatography (elution solvent: HEX-EtOAc) to obtain a crude purified product having ethyl 7-hydroxy-1,2,4,5-tetrahydro-3H-3-benzazepine-3-carboxylate as a main component. The crude purified product was recrystallized from ethyl acetate twice to obtain 15.66 g of ethyl 7-hydroxy-1,2,4,5-tetrahydro-3H-3-benzazepine-3-carboxylate.
後処理
- temperaturecooling
- stirringby stirring at the same temperature for 0.5 hours
- stirringstirring at 60° C. for 3 hours
- extractionThe reaction mixture was extracted with ethyl acetate
- dry with materialthe organic layer was dried over anhydrous magnesium sulfate
- filtrationfiltered
- concentrationthe filtrate was concentrated under reduced pressure
- customThe residue was purified by silica gel chromatography (elution solvent: HEX-EtOAc)
- customto obtain a crude
- custompurified product
- customThe crude purified product
- customwas recrystallized from ethyl acetate twice
出典と根拠
- ORDレコード
- ord-52a6c34f8794481f94791125560df3f2
- 出典データセット
- uspto-grants-2015_08
- 特許番号
- US09108977B2
反応ノート
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