反応式
[CH3:1][NH:2][CH2:3][CH2:4][CH3:5].[CH3:6][O:7][C:8](=[O:19])[C:9]1[CH:17]=[C:16]([Br:18])[CH:15]=[C:11]([C:12]([OH:14])=O)[CH:10]=1.BrC1C=C(C(O)=O)C=C(C=1)C(O)=O.ON1C2C=CC=CC=2N=N1.Cl.CN(C)CCCN=C=NCC.[Cl-].[NH4+].Cl>ClCCl>[CH3:6][O:7][C:8](=[O:19])[C:9]1[CH:17]=[C:16]([Br:18])[CH:15]=[C:11]([C:12]([N:2]([CH3:1])[CH2:3][CH2:4][CH3:5])=[O:14])[CH:10]=1参加物
反応物 7
生成物 1
試薬・触媒・溶媒 1
実験手順
Add N-methylpropylamine (5.14 g, 70.4 mmol) to a mixture of 5-bromo-isophthalic acid monomethyl ester and 5-bromo-isophthalic acid (18.2 g), 1-hydroxybenzotriazole (9.5 g, 70.4 mmol), and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (13.5 g, 70.4 mmol) in dichloromethane (200 mL). Stir the solution for 2 h at room temperature. Add saturated aqueous ammonium chloride (100 mL) and acidify the mixture with 1 N HCl. Filter away the precipitate, extract the filtrate with dichloromethane, wash the organic extracts with 1 N HCl, saturated aqueous sodium bicarbonate, saturated aqueous sodium chloride, dry (magnesium sulfate), concentrate and purify (silica gel chromatography, eluting with 30:70 ethyl acetate:hexanes) to give the title compound as an oil (10.1 g, 46%).
後処理
- filtrationFilter away the precipitate
- extractionextract the filtrate with dichloromethane
- washwash the organic extracts with 1 N HCl, saturated aqueous sodium bicarbonate, saturated aqueous sodium chloride
- dry with materialdry (magnesium sulfate)
- concentrationconcentrate
- custompurify
- wash(silica gel chromatography, eluting with 30:70 ethyl acetate:hexanes)
出典と根拠
- ORDレコード
- ord-b4a49b99652d405b815196d3ea594cff
- 出典データセット
- uspto-grants-2009_11
- 特許番号
- US07618978B2
関連ノート
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