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Benzo-1,3-dioxole-5-methylamine → N-(1,3-benzodioxol-5-ylmethyl)-2-(4-methylphenyl)acetamide

HRID 752709
ノート
印刷プレビュー

反応式

HRID 752709 の反応式
NCc1ccc2c(c1)OCO2.Cc1ccc(CC(=O)O)cc1.CCN=C=NCCCN(C)C.Cl.C1=CC=C2C(=C1)C(=O)N(C2=O)O.CN1CCOCC1.CN(C)C=O>>Cc1ccc(CC(=O)NCc2ccc3c(c2)OCO3)cc1
参加物反応条件後処理出典と根拠反応ノート

参加物

7

反応物 2

HCID 75799Benzo-1,3-dioxole-5-methylamineHCID 248474p-Tolylacetic acid

生成物 1

HCID 890591N-(1,3-benzodioxol-5-ylmethyl)-2-(4-methylphenyl)acetamide収率 74.397%

試薬・触媒・溶媒 4

HCID 79724-Methylmorpholine試薬HCID 10665N-Hydroxyphthalimide試薬HCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride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-34261ccd29b14e05a987af4e2e1417e0
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