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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 18784188, 화합물 → HCID 69973134, 화합물

HRID 1108770
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반응식

HRID 1108770 반응식
[ClH:1].C([NH:9][CH2:10][CH:11]1[CH2:15][CH2:14][CH:13]([C:16]2[CH:21]=[CH:20][C:19]([O:22][CH3:23])=[CH:18][CH:17]=2)[CH2:12]1)C1C=CC=CC=1.[H][H]>C(O)(=O)C.[C].[Pd]>[ClH:1].[CH3:23][O:22][C:19]1[CH:20]=[CH:21][C:16]([CH:13]2[CH2:14][CH2:15][CH:11]([CH2:10][NH2:9])[CH2:12]2)=[CH:17][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 18784188HCID 18784188, 화합물HCID 178418361HCID 178418361, 화합물2회

생성물 1

HCID 69973134HCID 69973134, 화합물수율 94%

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 176Acetic Acid용매

실험 절차

N-Benzyl-N-[3-(4-methoxyphenyl)cyclopentylmethyl]amine hydrochloride (6.30 g) was dissolved in acetic acid (130 ml), and 10% palladium-carbon (1.1 g) was added. After substituting the reaction vessel with hydrogen gas, hydrogen addition was carried out at normal pressure, 80° C. for 2 hours. After the reaction, the catalyst was filtered off and the solvent was distilled off under reduced pressure to produce light yellow crystals which were then washed with diethyl ether to give 4.31 g of 3-(4-methoxyphenyl) cyclopentylmethylamine hydrochloride (94.0%).

후처리

  1. customAfter the reaction
  2. filtrationthe catalyst was filtered off
  3. distillationthe solvent was distilled off under reduced pressure
  4. customto produce light yellow crystals which
  5. washwere then washed with diethyl ether

출처 및 근거

ORD 기록
ord-f6485d7a50794c76943ba7e2ab3094b4
출처 데이터셋
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06069176

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