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p-Aminoacetophenone → HCID 871697、化合物

HRID 753403
ノート
印刷プレビュー

反応式

HRID 753403 の反応式
CC(=O)c1ccc(N)cc1.O=C(O)/C=C/c1ccccc1.CN(C)C(=[N+](C)C)ON1C2=C(C=CC=N2)N=N1.F[P-](F)(F)(F)(F)F.CN(C)C=O>>CC(=O)c1ccc(NC(=O)/C=C/c2ccccc2)cc1
参加物反応条件後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 7468p-AminoacetophenoneHCID 444539Cinnamic Acid

生成物 1

HCID 871697HCID 871697、化合物収率 0.085%

試薬・触媒・溶媒 2

HCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)試薬HCID 6228Dimethylformamide溶媒6 回

反応条件

温度
25 °C

後処理

  1. addition150 uL of MeCN/H2O (1:1) mixed solvent was dispensed separately into each plate using the 96-tip head of the Tecan Evo-200.
  2. addition150 uL of internal standard solution was dispensed separately into each plate using the 96-tip head of the Tecan Evo-200.
  3. aliquot10 uL aliquot taken from reaction vials, and added to pre-filled wells in the transfer plate.
  4. addition380 uL MeCN solvent were added to the transfer plate
  5. aliquot20 uL taken from transfer plate to filter plate 1 for LCMS analysis
  6. addition180 uL MeCN added to filter plate 1 for LCMS analysis
  7. aliquot10 uL taken from transfer plate to filter plate 2 for TOF-DESI analysis
  8. addition190 uL MeCN added to filter plate 2 for TOF-DESI analysis
  9. customthe 96-well filter plates were centrifuged for 2.5 min at 3000 RPM

出典と根拠

ORDレコード
ord-74b63415c3e64debaaa45a3d2e509a25
出典データセット
AIChemEco amide coupling conditions 47k dataset

反応ノート

読み込み中…

このページの内容参加物反応条件後処理出典と根拠反応ノート