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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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(1,4-Dibenzylpiperazin-2-yl)-N,N-dimethylmethanamine → N,N-dimethyl-2-piperazinemethanamine

HRID 1988985
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HRID 1988985 반응식
C([N:8]1[CH2:13][CH2:12][N:11](CC2C=CC=CC=2)[CH2:10][CH:9]1[CH2:21][N:22]([CH3:24])[CH3:23])C1C=CC=CC=1>CCO.[Pd]>[CH3:23][N:22]([CH3:24])[CH2:21][CH:9]1[CH2:10][NH:11][CH2:12][CH2:13][NH:8]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 14664170(1,4-Dibenzylpiperazin-2-yl)-N,N-dimethylmethanamine

생성물 1

HCID 14664185N,N-dimethyl-2-piperazinemethanamine

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

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온도
130 °C

실험 절차

{[1,4-bisbenzylpiperazin-2-yl]methyl}dimethylamine (1 equivalent), was dissolved in EtOH and the solution was transferred to a stainless steel high pressure vessel equipped with a pressure gauge. 10% Pd/C was added (10 wt. %), and the vessel charged with H2. The reaction mixture was stirred at 130° C. and 200 psi of H2 overnight. The reaction mixture was cooled to room temperature, filtered over a pad of Celite, and then evaporated. The desired amine was obtained in quantitative yield as a pale yellow oil. GC/MS: 143 (10%, M+), Rt=14.3 minutes.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. customthe solution was transferred to a stainless steel high pressure vessel
  2. customequipped with a pressure gauge
  3. additionthe vessel charged with H2
  4. custom200 psi of H2 overnight
  5. temperatureThe reaction mixture was cooled to room temperature
  6. filtrationfiltered over a pad of Celite
  7. customevaporated

출처 및 근거

ORD 기록
ord-b8cff0ae258a431bac6dce3aee5c0250
출처 데이터셋
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07642278B2

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