3-Bromoquinoline → HCID 178519901、化合物

HRID 918700ノート

反応式

HRID 918700 の反応式
Brc1cnc2ccccc2c1.OCc1cocn1>CS(=O)(=O)O[Pd]c1ccccc1-c2ccccc2N.CC(C)Oc3cccc(OC(C)C)c3-c4ccccc4P(C5CCCCC5)C6CCCCC6.C(=O)([O-])[O-].[Cs+].[Cs+].C1COCCO1.[Cu]Br.CSC>OCc1coc(-c2cnc3ccccc3c2)n1.OCc1ncoc1-c1cnc2ccccc2c1.OCc1nc(-c2cnc3ccccc3c2)oc1-c1cnc2ccccc2c1

参加物

9

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-c581ff6883b04eba9dbdcd5e10160be4
出典データセット
C-H activation of oxazoles from the second demo case in the PyParser paper

反応ノート

読み込み中…