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3-Bromoquinoline → HCID 178519901、化合物

HRID 918711
ノート
印刷プレビュー

反応式

HRID 918711 の反応式
Brc1cnc2ccccc2c1.OCc1cocn1>Cl[Pd]Cl.Clc1cccnc1.CC(C)c2cccc(C(C)C)c2N3CN(C=C3)c4c(cccc4C(C)C)C(C)C.C(=O)([O-])[O-].[Cs+].[Cs+].C1COCCO1.[Cu]Br.CSC>OCc1coc(-c2cnc3ccccc3c2)n1.OCc1ncoc1-c1cnc2ccccc2c1.OCc1nc(-c2cnc3ccccc3c2)oc1-c1cnc2ccccc2c1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

9

反応物 2

HCID 214133-BromoquinolineHCID 159305781,3-Oxazol-4-ylmethanol

生成物 3

HCID 178519901HCID 178519901、化合物HCID 178519952HCID 178519952、化合物HCID 178520002HCID 178520002、化合物

試薬・触媒・溶媒 4

HCID 10796Cesium carbonate試薬HCID 2724234Bromo(thiobis(methane))copper

反応条件

温度
100 °C

実験手順

- reaction input `pd_catalyst` was added as a solution (2-methyltetrahydrofuran 1 mmol/L) and then the solvent was removed to leave solid solute before adding other reactants/reagents; - stirrer was added after `pd_catalyst` and before `base`; - reaction inputs were prepared inside a glove box but the reaction itself did not happen in a glove box; - the reaction vial was sealed after adding all reaction inputs

後処理

  1. temperatureThe reactions were then allowed to cool to room temperature
  2. additionEach reaction vial was diluted with 500 uL of a pre-prepared solution consisting of 1 umol dibenzylaniline (labelled as an internal standard for the purposes of PyParse analysis) and 20 umol dimethylsulfoxide in acetonitrile.
  3. stirringThe reactions were sealed and shaken to ensure a homogenous mixture.
  4. aliquot50 uL of each reaction mixture was then aspirated and dispensed to the analysis plate.
  5. additionEach well of the analysis plate was diluted with 150 uL of dimethylsulfoxide, and the analysis plate was sealed with polypropylene film.

出典と根拠

ORDレコード
ord-779d9cad8bd84b3d96432eb1e713fc1a
出典データセット
C-H activation of oxazoles from the second demo case in the PyParser paper
DOI
10.1039/d3dd00167a

反応ノート

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