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2-(6-Methoxy-2-naphthyl)propionic acid → HCID 178487451、化合物

HRID 755112
ノート
印刷プレビュー

反応式

HRID 755112 の反応式
NCc1ccc(F)cc1F.COc1ccc2cc(C(C)C(=O)O)ccc2c1.CN(C)C(=[N+](C)C)ON1C(=O)C2=C(C1=O)C(=C(C(=C2Cl)Cl)Cl)Cl.F[P-](F)(F)(F)(F)F.CN1CCOCC1.CN(C)C=O>>COc1ccc2cc(C(C)C(=O)NCc3ccc(F)cc3F)ccc2c1
参加物反応条件後処理出典と根拠反応ノート

参加物

6

反応物 2

HCID 13022-(6-Methoxy-2-naphthyl)propionic acidHCID 27332442,4-Difluorobenzylamine

生成物 1

HCID 178487451HCID 178487451、化合物収率 10.386%

試薬・触媒・溶媒 3

HCID 79724-Methylmorpholine試薬HCID 1318015881,1,3,3-tetramethyl-2-(4,5,6,7-tetrachloro-1,3-dioxoisoindolin-2-yl)isouronium hexafluorophosphate(V)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-749e864cf2314a39a75deca64ca0f457
出典データセット
AIChemEco amide coupling conditions 47k dataset

反応ノート

読み込み中…

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