Hydrochloric Acid → HCID 19095386、化合物
反応式
C[O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[N:10]([CH2:14][CH2:15][NH:16][C:17](=[O:19])[CH3:18])[CH:11]=[CH:12][CH:13]=2)=[CH:5][CH:4]=1.B(Br)(Br)Br.[OH-].[Na+].Cl>C(Cl)Cl>[OH:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[N:10]([CH2:14][CH2:15][NH:16][C:17](=[O:19])[CH3:18])[CH:11]=[CH:12][CH:13]=2)=[CH:5][CH:4]=1参加物
反応条件
- 温度
- -15 °C
実験手順
N-[2-[2-(p-Methoxyphenyl)pyrrol-1-yl]ethyl]acetamide (10.4 g) was dissolved in 300 ml of methylene chloride under argon, cooled to -15° C. and treated at this temperature while stirring with a solution of 11.6 ml of boron tribromide in 90 ml of methylene chloride. The mixture was stirred at -15° C. for 1 hour, at 0° C. for 2 hours and at room temperature overnight. The reaction mixture was treated at -10° C. with 270 ml of 2N sodium hydroxide solution and stirred at room temperature for 1 hour. 200 ml of methylene chloride were added to this mixture and the resulting mixture was adjusted to pH=8 with 70 ml of 2N hydrochloric acid. The phases were separated and the aqueous phase was extracted twice with 150 ml of methylene chloride each time. The organic phases were combined, dried with MgSO4 and freed from solvent. The residue, 8.2 g of brown oil, was chromatographed on 250 g of silica gel with methylene chloride/methanol mixtures (50:1 to 20:1) as the eluent. There were obtained 5.4 g (55%) of N-[2 -[2-(p-hydroxyphenyl)pyrrol-1-yl]ethyl]acetamide as a colourless, amorphous solid which was processed without further purification. MS: (m/e)=244 (M+).
後処理
- additiontreated at this temperature
- stirringstirred at room temperature for 1 hour
- customThe phases were separated
- extractionthe aqueous phase was extracted twice with 150 ml of methylene chloride each time
- dry with materialdried with MgSO4
- customThe residue, 8.2 g of brown oil, was chromatographed on 250 g of silica gel with methylene chloride/methanol
出典と根拠
- ORDレコード
- ord-adaa85d857ba49cb88ffbb6bdbf786bf
- 出典データセット
- uspto-grants-1994_03
- 特許番号
- US05292732
反応ノート
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