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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-Phenylpiperidine → 3-(4-Phenyl-1-piperidinyl)pyridine

HRID 1344741
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인쇄 미리보기

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HRID 1344741 반응식
Ic1cccnc1.c1ccc(C2CCNCC2)cc1>CS(C)=O.Cc1cc(O)cc(C)c1NC(=O)C(=O)Nc1c(C)cc(O)cc1C.O=C([O-])[O-].[Cs+].[Cu][O][Cu]>c1ccc(C2CCN(c3cccnc3)CC2)cc1
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참가 물질

9

반응물 2

HCID 698734-PhenylpiperidineHCID 707143-Iodopyridine

생성물 3

HCID 2519CaffeineHCID 1223802233-(4-Phenyl-1-piperidinyl)pyridine수율 0%HCID 1398883374-(4-Phenylpiperidin-1-yl)pyridine수율 0%

시약·촉매·용매 4

HCID 14794698CID 14794698시약HCID 126500385N1,N2-bis(4-hydroxy-2,6-dimethylphenyl)oxalamide촉매HCID 178505380HCID 178505380, 화합물촉매HCID 679Dimethyl Sulfoxide용매5회

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온도
60 °C

후처리

  1. customThe foil sealing tape was removed from the plate.
  2. addition3 μL of a 0.0667 M solution of caffeine in DMSO was added to each reaction well using an SPT Labtech Mosquito® liquid handling robot
  3. filtrationThe plates were then centrifuged for 15 to 20 seconds. · liquid 상 유지
  4. aliquotFollowing centrifugation, 500 nL of the resultant mixture from each well was carefully dispensed into four 384-well analytical plates (Analytical Sales # 38435) using an SPT Labtech Mosquito® liquid handling robot. Each well of these analytical plates contained 30 μL of DMSO with 0.1% acetic acid, pre-dosed by OpenTrons, to facilitate analysis.

출처 및 근거

ORD 기록
ord-ae8c0eb4431b4767bf3016099f3bd1df
출처 데이터셋
High-throughput exploration of 50,688 Pd-, Ni- and Cu-catalysed C–N coupling reactions
DOI
10.1021/jacs.6c05959
원본 링크
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