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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 66744472, 화합물 → HCID 66744159, 화합물

HRID 505111
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HRID 505111 반응식
C([N:8]1[CH2:13][CH:12]=[C:11]([C:14]2[C:22]3[O:21][CH2:20][CH2:19][C:18]=3[CH:17]=[C:16](Br)[CH:15]=2)[CH2:10][CH2:9]1)C1C=CC=CC=1>CCO.Cl.[Pd]>[O:21]1[C:22]2[C:14]([CH:11]3[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]3)=[CH:15][CH:16]=[CH:17][C:18]=2[CH2:19][CH2:20]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 66744472HCID 66744472, 화합물

생성물 1

HCID 66744159HCID 66744159, 화합물수율 81%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 313Hydrochloric Acid용매HCID 702Ethanol용매

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온도
50 °C

실험 절차

To a solution of 1-benzyl-4-(5-bromo-2,3-dihydro-benzofuran-7-yl)-1,2,3,6-tetrahydro-pyridine in EtOH and 4N HCl was added 40 wt % of 10% Pd/C catalyst. The reaction flask was charged with H2 (3.5 bar) and then stirred overnight at 50° C. The reaction mixture was filtered over Celite under argon. The solvents were evaporated and the product was partitioned between CH2Cl2 and aq. K2CO3. The organic phase was dried over Na2SO4 and evaporated to give the title compound in 81% yield.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. additionThe reaction flask was charged with H2 (3.5 bar)
  2. filtrationThe reaction mixture was filtered over Celite under argon
  3. customThe solvents were evaporated
  4. customthe product was partitioned between CH2Cl2 and aq. K2CO3
  5. dry with materialThe organic phase was dried over Na2SO4
  6. customevaporated

출처 및 근거

ORD 기록
ord-765690d0e20d4bfba243719867f03c67
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07781436B2

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