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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → 2,8a-dibenzyl-1,2,3,4,8,8a-hexahydroisoquinolin-6(7H)-one

HRID 1042322
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HRID 1042322 반응식
[CH2:1]([N:8]1[CH2:13][CH2:12][C:11](=O)[CH:10]([CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C[O-].[Na+].[CH3:25][C:26]([CH:28]=[CH2:29])=[O:27].Cl>CO>[CH2:1]([N:8]1[CH2:13][CH2:12][C:11]2[C:10]([CH2:15][C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)([CH2:29][CH2:28][C:26](=[O:27])[CH:25]=2)[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
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참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 6570Methyl vinyl ketoneHCID 10942334Sodium MethoxideHCID 230036591,3-Dibenzylpiperidin-4-one

생성물 1

HCID 444429102,8a-dibenzyl-1,2,3,4,8,8a-hexahydroisoquinolin-6(7H)-one

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

1,3-Dibenzylpiperidin-4-one (3, R1B=H, Z=benzyl) (3.98 g, 13.96 mmol) was added to a solution of sodium methoxide (0.83 g, 15.36 mmol) in 80 mL of methanol and stirred at ambient temperature for 45 min. The contents were cooled to 0° C. and methylvinyl ketone (1.74 mL, 20.94 mmol) was added over 30 min. The contents were allowed to warm to ambient temperature and stir for 18 h. Concentrated HCl (1.55 mL) was added, the contents were stirred for a further 5 min and the solvents were evaporated to give a brown oil which was triturated in diethyl ether to give the title compound, 1.90 g. LC-MS: RT=2.26 min. (M+H)+ 332.

후처리

  1. temperatureThe contents were cooled to 0° C.
  2. temperatureto warm to ambient temperature
  3. stirringstir for 18 h
  4. stirringthe contents were stirred for a further 5 min
  5. customthe solvents were evaporated
  6. customto give a brown oil which
  7. customwas triturated in diethyl ether

출처 및 근거

ORD 기록
ord-78622167dabc420eae04c95e2ab3355b
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08557839B2

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