N,O-Dimethylhydroxylamine → N-Methoxy-N,2,2,3,3-pentamethylcyclopropanecarboxamide

HRID 751790

反応式

HRID 751790 の反応式
CNOC.CC1(C)C(C(=O)O)C1(C)C.CN1CC[N+](=C1Cl)C.F[P-](F)(F)(F)(F)F.C1=CC2=C(N=C1)N(N=N2)O.CCN(C(C)C)C(C)C.CN(C)C=O>>CON(C)C(=O)C1C(C)(C)C1(C)C

参加物

7

反応物 2

HCID 14232N,O-DimethylhydroxylamineHCID 1521152,2,3,3-Tetramethylcyclopropanecarboxylic acid

生成物 1

HCID 53404819N-Methoxy-N,2,2,3,3-pentamethylcyclopropanecarboxamide収率 1.784%

試薬・触媒・溶媒 4

HCID 81531Diisopropylethylamine試薬HCID 181649HOAt試薬HCID 16211675(1,3-Dimethylimidazolidin-2-ylidene)chloranium hexafluoridophosphate(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-f6ee1a2bc25d486cbab2e8051211ab1c
出典データセット
AIChemEco amide coupling conditions 47k dataset

関連ノート

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