1-(3,5-Dimethylphenyl)ethan-1-one → Biphenyl

HRID 438300

反応式

HRID 438300 の反応式
CC(=O)c1cc(C)cc(C)c1.CN[C@@H]1C[C@H]2O[C@@](C)([C@@H]1OC)n1c3ccccc3c3c4c(c5c6ccccc6n2c5c31)C(=O)NC4>CC(=O)N(C)C.CC(=O)O.CC(=O)O[BH-](OC(C)=O)OC(C)=O.CC(C)[O-].CC(C)[O-].CC(C)[O-].CC(C)[O-].[Na+].[Ti+4]>CO[C@@H]1[C@H](N(C)C(C)c2cc(C)cc(C)c2)C[C@H]2O[C@]1(C)n1c3ccccc3c3c4c(c5c6ccccc6n2c5c31)C(=O)NC4

参加物

10

反応物 2

HCID 149211-(3,5-Dimethylphenyl)ethan-1-oneHCID 44259Staurosporine

生成物 4

HCID 7095BiphenylHCID 44259StaurosporineHCID 53694894-Phenyl-3-buten-2-ol, (3E)-HCID 178496705HCID 178496705、化合物

試薬・触媒・溶媒 4

HCID 176Acetic Acid試薬HCID 11026Titanium isopropoxide試薬HCID 5049666Sodium triacetoxyborohydride試薬HCID 31374Dimethylacetamide溶媒7 回

反応条件

温度
22 °C

後処理

  1. additionThe next morning, the Mosquito(R) was used to dilute the 100 mM reactions to 50 mM via addition of 1 uL DMSO to each reaction well, followed by dispense mixing.
  2. additionThe reactions were diluted with 3x1 uL DMSO (containing PhPh as an internal standard) using the Mosquito(R). The reactions were mixed after each dispense operation.
  3. aliquotMosquito(R) was used to transfer 1 uL of each quenched reaction from the 1,536-well reaction plate to 384-well analytical plates containing 60 uL DMSO for analysis by UPLC.
  4. additionMosquito(R) was used to transfer 1 uL of each quenched reaction from the 1,536-well reaction plate to 384-well analytical plates containing 60 uL DMSO for analysis by UPLC.

出典と根拠

ORDレコード
ord-867d34b7d5d3446c9960851566f32c53
出典データセット
Cernak miniaturized reductive amination
元リンク
出典を表示

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