3-Bromoquinoline → HCID 178519901、化合物
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
反応物 2
生成物 3
試薬・触媒・溶媒 4
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
- temperatureThe reactions were then allowed to cool to room temperature
- 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.
- stirringThe reactions were sealed and shaken to ensure a homogenous mixture.
- aliquot50 uL of each reaction mixture was then aspirated and dispensed to the analysis plate.
- 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…