反応式
[CH3:1][CH:2]([N:4]([CH2:8][CH2:9][N:10]1C(=O)C2C(=CC=CC=2)C1=O)[CH:5]([CH3:7])[CH3:6])[CH3:3].O.NN.C1(N)C(F)=C(F)C(F)=C(N)C=1F.[ClH:36].Cl>C(O)C.CO>[ClH:36].[ClH:36].[CH3:1][CH:2]([N:4]([CH:5]([CH3:7])[CH3:6])[CH2:8][CH2:9][NH2:10])[CH3:3]参加物
実験手順
A solution of 40.54 g (0.148 mole) of 2-[2-[[N,N-bis(1-methylethyl)amino]ethyl]-2H-isoindole-1,3-dione and hydrazine hydrate (85%, 11.8 g, 0.2 mole) in 400 ml of 95% ethanol was heated at reflux for 5 hours. The reaction mixture was allowed to cool to room temperature while standing overnight. A white solid formed. The reaction mixture was concentrated almost to dryness on the rotary evaporator. The residue was dissolved in chloroform and extracted with 10% sodium hydroxide. After removing chloroform, a brown oil was obtained. A portion of the oil was dissolved in methanol and converted to the dihydrochloride salt. After recrystallization from methanol-diethyl ether, 1.50 g (20%) of white crystalline product, m.p. 178°-182° C. (decomposition) was obtained.
後処理
- temperatureat reflux for 5 hours
- customA white solid formed
- concentrationThe reaction mixture was concentrated almost to dryness on the rotary evaporator
- dissolutionThe residue was dissolved in chloroform
- extractionextracted with 10% sodium hydroxide
- customAfter removing chloroform
- customa brown oil was obtained
- customAfter recrystallization from methanol-diethyl ether, 1.50 g (20%) of white crystalline product
- customm.p. 178°-182° C. (decomposition) was obtained
出典と根拠
- ORDレコード
- ord-14a1b474b9c541c497a63eeb1cc0257c
- 出典データセット
- uspto-grants-1986_07
- 特許番号
- US04597902
関連ノート
読み込み中…