Benzene → 1-(2-Amino-4-chlorophenyl)-5-chloroindoline hydrochloride ethanolate

HRID 4062

反応式

HRID 4062 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([C:11]1[CH:16]=[CH:15][C:14]([Cl:17])=[CH:13][C:12]=1[N+:18]([O-])=[O:19])[CH2:6][CH2:5]2.[CH:21]1[CH:26]=CC=CC=1>[Pt].C(O)C>[CH2:26]([O-:19])[CH3:21].[ClH:1].[NH2:18][C:12]1[CH:13]=[C:14]([Cl:17])[CH:15]=[CH:16][C:11]=1[N:7]1[C:8]2[C:4](=[CH:3][C:2]([Cl:1])=[CH:10][CH:9]=2)[CH2:5][CH2:6]1

参加物

5

実験手順

A Parr bottle, charged with 12.4 g (0.040 mole) of 5-chloro-1-(4-chloro-2-nitrophenyl)indoline of Example 8a, 100 ml of benzene, 100 ml of absolute ethanol and 0.5 g of 1% Pt/C was shaken under an initial hydrogen pressure of 57 psig until uptake ceased. The catalyst was then removed by filtration and the filtrate was concentrated in vacuo to an oil weighing 11.2 g (100%). This was dissolved in 30 ml of ethanol and then 30 ml of ether saturated with hydrogen chloride was added. An additional 500 ml of plain ether was added, and the mixture was stirred at 0° C., to maximize precipitation. The hydrochloride salt was collected, dried, and found to weigh 9.2 g (73%), m.p. 174°-178° C. Recrystallization from ethanol (charcoal) afforded 1-(2-amino-4-chlorophenyl)-5-chloroindoline hydrochloride ethanolate in 58% overall yield, m.p. 177°-180° C.

後処理

  1. customThe catalyst was then removed by filtration
  2. concentrationthe filtrate was concentrated in vacuo to an oil
  3. dissolutionThis was dissolved in 30 ml of ethanol
  4. addition30 ml of ether saturated with hydrogen chloride was added
  5. additionAn additional 500 ml of plain ether was added
  6. stirringthe mixture was stirred at 0° C.
  7. customprecipitation
  8. customThe hydrochloride salt was collected
  9. customdried
  10. customRecrystallization from ethanol (charcoal)

出典と根拠

ORDレコード
ord-045e2fa84c854fe2b6a46ce09d53e1c2
出典データセット
uspto-grants-1988_02
特許番号
US04723003

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