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Diisopropylethylamine → HCID 44227500、化合物

HRID 1914576
ノート
印刷プレビュー

反応式

HRID 1914576 の反応式
[NH:1]1[CH:5]=[C:4]([C:6]2[S:10][CH:9]=[C:8]([C:11]([OH:13])=O)[CH:7]=2)[CH:3]=[N:2]1.CCN(C(C)C)C(C)C.[F:23][C:24]([F:37])([F:36])[CH2:25][N:26]1[CH:35]2[CH:30]([CH2:31][CH2:32][CH2:33][CH2:34]2)[NH:29][CH2:28][CH2:27]1.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F>C(#N)C>[NH:2]1[CH:3]=[C:4]([C:6]2[S:10][CH:9]=[C:8]([C:11]([N:29]3[CH:30]4[CH:35]([CH2:34][CH2:33][CH2:32][CH2:31]4)[N:26]([CH2:25][C:24]([F:36])([F:37])[F:23])[CH2:27][CH2:28]3)=[O:13])[CH:7]=2)[CH:5]=[N:1]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 81531Diisopropylethylamine2 回HCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)2 回HCID 581101935-(1H-Pyrazol-4-YL)thiophene-3-carboxylic acidHCID 58110330HCID 58110330、化合物

生成物 1

HCID 44227500HCID 44227500、化合物収率 12.2%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

5-(1H-Pyrazol-4-yl)-thiophene-3-carboxylic acid (0.080 g, 0.41 mmol) was suspended in acetonitrile (2 mL) then DIPEA (0.158 mL, 0.90 mmol) and 1-(2,2,2-trifluoro-ethyl)-decahydro-quinoxaline (0.119 g, 0.54 mmol) were added followed by HATU (0.192 g, 0.50 mmol). The resulting mixture was stirred for about 24 hours and then further amounts of DIPEA (79 μL) and HATU (0.192 g) were added and stirring continued over the weekend. The mixture was evaporated and the residue was taken up in sodium hydroxide (1 N) and stirred for 30 minutes. HCl (1 N, 2.5 mL) was added and the solution extracted with ethyl acetate (×3). The organics were dried over sodium sulfate, filtered and evaporated. The material was purified by HPLC, eluting with 5%-95% acetonitrile in water (0.1% formic acid) and the fractions containing the desired product were combined and freeze-dried to give the title compound as a white solid (0.020 g). LCMS m/z 399.17 [M+H]+ R.T.=10.05 min (Analytical Method 2).

後処理

  1. stirringstirring
  2. customThe mixture was evaporated
  3. stirringstirred for 30 minutes
  4. additionHCl (1 N, 2.5 mL) was added
  5. extractionthe solution extracted with ethyl acetate (×3)
  6. dry with materialThe organics were dried over sodium sulfate
  7. filtrationfiltered
  8. customevaporated
  9. customThe material was purified by HPLC
  10. washeluting with 5%-95% acetonitrile in water (0.1% formic acid)
  11. additionthe fractions containing the desired product
  12. customfreeze-dried

出典と根拠

ORDレコード
ord-ffd1ba6003874fe889eb0fe411216b5d
出典データセット
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08614209B2

反応ノート

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