Hydrazine hydrate (1:1) → N,N-bis(1-Methylethyl)-1,2-ethanediamine, dihydrochloride

HRID 745171

반응식

HRID 745171 반응식
[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]

참가 물질

6

실험 절차

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.

후처리

  1. temperatureat reflux for 5 hours
  2. customA white solid formed
  3. concentrationThe reaction mixture was concentrated almost to dryness on the rotary evaporator
  4. dissolutionThe residue was dissolved in chloroform
  5. extractionextracted with 10% sodium hydroxide
  6. customAfter removing chloroform
  7. customa brown oil was obtained
  8. customAfter recrystallization from methanol-diethyl ether, 1.50 g (20%) of white crystalline product
  9. customm.p. 178°-182° C. (decomposition) was obtained

출처 및 근거

ORD 기록
ord-14a1b474b9c541c497a63eeb1cc0257c
출처 데이터셋
uspto-grants-1986_07
특허 번호
US04597902

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