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Hydrochloric Acid → HCID 13671866, 화합물

HRID 1655320
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HRID 1655320 반응식
[NH2:1][CH:2]([CH2:11][CH2:12][CH:13]([CH3:15])[CH3:14])[CH:3]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)[OH:4].[Cl:16][CH2:17][CH2:18][CH2:19][N:20]1[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]1.[ClH:26]>C(O)C>[ClH:16].[ClH:26].[CH3:14][CH:13]([CH3:15])[CH2:12][CH2:11][CH:2]([NH:1][CH2:17][CH2:18][CH2:19][N:20]1[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]1)[CH:3]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)[OH:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 79625Piperidine, 1-(3-chloropropyl)-HCID 13671865HCID 13671865, 화합물

생성물 1

HCID 13671866HCID 13671866, 화합물수율 33%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of (1RS,2SR)-2-amino-5-methyl-1-phenylhexan-1-ol (415 mg, 2 mmol) and 1-(3-chloropropyl)piperidine (324 mg, 2 mmol) was melted at 70° C. in a nitrogen atmosphere. The mixture was heated at 110° to 120° C. for 3 hours. After being cooled, the reaction mixture was dissolved with heating in ethanol, followed by addition of concentrated hydrochloric acid (0.2 ml). After the mixture was cooled, precipitated crystals were collected by filtration and washed with ethanol. The crystals were recrystallized from ethanol to obtain 0.27 g of the title compound as white crystals (yield: 33%).

후처리

  1. temperatureThe mixture was heated at 110° to 120° C. for 3 hours
  2. temperatureAfter being cooled
  3. dissolutionthe reaction mixture was dissolved
  4. temperatureAfter the mixture was cooled
  5. customprecipitated crystals
  6. filtrationwere collected by filtration
  7. washwashed with ethanol
  8. customThe crystals were recrystallized from ethanol

출처 및 근거

ORD 기록
ord-7618965cde3a48718346dd9085f10d57
출처 데이터셋
uspto-grants-1993_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05250546

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