Hydrazine hydrate (1:1) → [4-(6-aminomethyl-1H-inden-2-yl)-butyl]-dipropyl-amine

HRID 2080740노트

반응식

HRID 2080740 반응식
[CH2:1]([N:4]([CH2:28][CH2:29][CH3:30])[CH2:5][CH2:6][CH2:7][CH2:8][C:9]1[CH2:17][C:16]2[C:11](=[CH:12][CH:13]=[C:14]([CH2:18][N:19]3C=C4C(C=CC=C4)=C3)[CH:15]=2)[CH:10]=1)[CH2:2][CH3:3].O.NN>CO>[NH2:19][CH2:18][C:14]1[CH:15]=[C:16]2[C:11]([CH:10]=[C:9]([CH2:8][CH2:7][CH2:6][CH2:5][N:4]([CH2:28][CH2:29][CH3:30])[CH2:1][CH2:2][CH3:3])[CH2:17]2)=[CH:12][CH:13]=1

참가 물질

4

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 866149102-[2-(4-dipropylamino-butyl)-3H-inden-5-ylmethyl]-isoindol

생성물 1

HCID 23155401[4-(6-aminomethyl-1H-inden-2-yl)-butyl]-dipropyl-amine수율 65.2%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

The compound (82.0 mg) obtained in Example 11-12 was dissolved in methanol (4.1 ml) and added with hydrazine monohydrate (0.082 ml) and the whole was refluxed under heating for 3 hours. The reaction solution was concentrated under reduced pressure. Then, the residue was added with water and subjected to extraction with chloroform. The organic layer was washed with a saturated saline solution, dried with anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified through silica gel column chromatography (chloroform/ethyl acetate), thereby obtaining the subject compound (40.1 mg) as a yellow oily substance.

후처리

  1. temperaturethe whole was refluxed
  2. temperatureunder heating for 3 hours
  3. concentrationThe reaction solution was concentrated under reduced pressure
  4. additionThen, the residue was added with water
  5. extractionsubjected to extraction with chloroform
  6. washThe organic layer was washed with a saturated saline solution
  7. dry with materialdried with anhydrous sodium sulfate
  8. concentrationconcentrated under reduced pressure
  9. customThe residue was purified through silica gel column chromatography (chloroform/ethyl acetate)

출처 및 근거

ORD 기록
ord-c13f1557c993480daa9715a205cd9c4c
출처 데이터셋
uspto-grants-2011_04
특허 번호
US07932281B2

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