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HCID 59242664、化合物 → HCID 59242654、化合物

HRID 1630477
ノート
印刷プレビュー

反応式

HRID 1630477 の反応式
C(OC([N:8]1[CH2:13][CH2:12][N:11]([C:14]2[N:15]=[N:16][C:17]([C:27]([F:30])([F:29])[F:28])=[C:18]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=3[CH3:26])[CH:19]=2)[CH2:10][CH2:9]1)=O)(C)(C)C>CO>[N:11]1([C:14]2[N:15]=[N:16][C:17]([C:27]([F:29])([F:28])[F:30])=[C:18]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=3[CH3:26])[CH:19]=2)[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 59242664HCID 59242664、化合物

生成物 1

HCID 59242654HCID 59242654、化合物収率 50%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of 4-[5-(2-tolyl)-6-trifluoromethyl-pyridazin-3-yl]-piperazine-1-carboxylic acid tert-butyl ester (D11) (0.089 g, 0.21 mmol) in methanol (7 ml) was added Amberlyst® 15 ion exchange resin, acidic form (4.1 mmol/g) (0.257 g, 1.05 mmol) and the reaction mixture was shaken at room temperature for 18 h. After this period, the mixture was filtered and then a saturated solution of ammonia in methanol was added. The mixture was shaken for 1 h, filtered and the filtrate evaporated in vacuo. The residue was purified by HPLC and the desired fractions were collected and evaporated in vacuo to yield E8 (0.026 g, 50%) as a white solid. C16H17F3N4 requires 322; Found 323 (MH+).

後処理

  1. wait
After this period
  • filtrationthe mixture was filtered
  • additiona saturated solution of ammonia in methanol was added
  • stirringThe mixture was shaken for 1 h
  • filtrationfiltered
  • customthe filtrate evaporated in vacuo
  • customThe residue was purified by HPLC
  • customthe desired fractions were collected
  • customevaporated in vacuo
  • 出典と根拠

    ORDレコード
    ord-9b73c9e697c148b9868f043f8fe56ee2
    出典データセット
    uspto-grants-2014_07
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US08791120B2

    反応ノート

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