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Dichloromethane → 3-(4-Isopropyl-piperazin-1-yl)-propylamine

HRID 1986165
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HRID 1986165 반응식
NN.[CH:3]([N:6]1[CH2:11][CH2:10][N:9]([CH2:12][CH2:13][CH2:14][N:15]2C(=O)C3C(=CC=CC=3)C2=O)[CH2:8][CH2:7]1)([CH3:5])[CH3:4].ClCCl>C(O)C>[CH:3]([N:6]1[CH2:7][CH2:8][N:9]([CH2:12][CH2:13][CH2:14][NH2:15])[CH2:10][CH2:11]1)([CH3:5])[CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6344DichloromethaneHCID 9321HydrazineHCID 20252235N-[3-(4-isopropyl-1-piperazinyl)propyl]phthalimide

생성물 1

HCID 128029563-(4-Isopropyl-piperazin-1-yl)-propylamine

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Hydrazine (8.63 g, 270 mmol) is added to a stirred suspension of 2-[3-(4-isopropylpiperazin-1-yl)-propyl]-isoindole-1,3-dione (17.0 g, 53.9 mmol) in anhydrous ethanol (400 mL). The resultant mixture is heated in an oil bath at 75° C. for 16 hours. At ambient temperature, dichloromethane (300 mL) is added to the mixture and the suspension is allowed to stir for 10 minutes. After filtration and concentration, the title compound is obtained as a tan oil (8.12 g, 81% yield).

후처리

  1. filtrationAfter filtration and concentration

출처 및 근거

ORD 기록
ord-be701dd17359432ea03ad3c4cbef9645
출처 데이터셋
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07547691B2

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