Hydrazine hydrate (1:1) → 3-(3-(Piperidin-1-ylmethyl)phenoxy)propan-1-amine

HRID 1609460노트

반응식

HRID 1609460 반응식
[N:1]1([CH2:7][C:8]2[CH:9]=[C:10]([CH:26]=[CH:27][CH:28]=2)[O:11][CH2:12][CH2:13][CH2:14][N:15]2C(=O)C3=CC=CC=C3C2=O)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.O.NN>CO>[N:1]1([CH2:7][C:8]2[CH:9]=[C:10]([CH:26]=[CH:27][CH:28]=2)[O:11][CH2:12][CH2:13][CH2:14][NH2:15])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1

참가 물질

4

반응 조건

온도
70 °C

실험 절차

To a solution of 16.3 g of the N-[3-[3-(piperidinomethyl)phenoxy]propyl]phthalimide in 150 ml of methanol was added 2.3 g of hydrazine monohydrate, and the mixture was heated at 70° C. for 4 hours. The mixture was cooled, then the solvent was distilled off, 30 ml of 6N hydrochloric acid was added to the residue, and the mixture was heated at 60° C. for 15 minutes. The resulting mixture was cooled, the insolubles were then filtered off, the solution was made alkaline with potassium hydroxide and subjected to extraction with a mixture of ethyl acetate and diethyl ether (1:1), and the organic layer was dried over magnesium sulfate and thereafter distilled to remove the solvent, giving 8.3 g of pale yellow oily 3-[3-(1-piperidinomethyl)phenoxy]propylamine (yield 78% ).

후처리

  1. temperatureThe mixture was cooled
  2. distillationthe solvent was distilled off
  3. addition30 ml of 6N hydrochloric acid was added to the residue
  4. temperaturethe mixture was heated at 60° C. for 15 minutes
  5. temperatureThe resulting mixture was cooled
  6. filtrationthe insolubles were then filtered off
  7. extractionsubjected to extraction with a mixture of ethyl acetate and diethyl ether (1:1)
  8. dry with materialthe organic layer was dried over magnesium sulfate
  9. distillationdistilled
  10. customto remove the solvent

출처 및 근거

ORD 기록
ord-9a144552368646b29bf16aa0e1e8441b
출처 데이터셋
uspto-grants-1995_03
특허 번호
US05401739

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