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4-methoxythiophene-3-carboxylic acid → HCID 44540247、化合物

HRID 244734
ノート
印刷プレビュー

反応式

HRID 244734 の反応式
[CH3:1][O:2][C:3]1[C:4]([C:8]([OH:10])=O)=[CH:5][S:6][CH:7]=1.F[P-](F)(F)(F)(F)F.CN(C(ON1C2=NC=CC=C2N=N1)=[N+](C)C)C.[NH:35]1[C:43]2[C:38](=[C:39]([C:44]3[CH:45]=[C:46]([NH2:53])[C:47]4[CH:48]=[N:49][NH:50][C:51]=4[CH:52]=3)[CH:40]=[CH:41][CH:42]=2)[CH:37]=[CH:36]1>CN(C=O)C.CCN(C(C)C)C(C)C>[NH:35]1[C:43]2[C:38](=[C:39]([C:44]3[CH:52]=[C:51]4[C:47]([CH:48]=[N:49][NH:50]4)=[C:46]([NH:53][C:8]([C:4]4[C:3]([O:2][CH3:1])=[CH:7][S:6][CH:5]=4)=[O:10])[CH:45]=3)[CH:40]=[CH:41][CH:42]=2)[CH:37]=[CH:36]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 3

HCID 27783794-methoxythiophene-3-carboxylic acidHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 582680196-(1H-indol-4-yl)-1H-indazol-4-amine

生成物 1

HCID 44540247HCID 44540247、化合物

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒2 回
HCID 81531Diisopropylethylamine溶媒

実験手順

4-(Methyloxy)-3-thiophenecarboxylic acid (35 mg) was treated with N-[(dimethylamino)(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yloxy)methylidene]-N-methylmethanaminium hexafluorophosphate (84 mg) in DMF (250 μl) and DIPEA (69 μl). The reaction mixture was shaken for five min prior to treatment with 6-(1H-indol-4-yl)-1H-indazol-4-amine (25 mg) in DMF (250 μl). The reaction mixture was left to stand at 22° C. for 18 h. The solvent was removed in vacuo and the product re-dissolved in chloroform (0.3 ml) prior to application on to an aminopropyl SPE cartridge (0.5 g) that had been preconditioned with methanol and then chloroform. The product was eluted after 2 hr with ethyl acetate/methanol (1:1, 3 ml), and concentrated under a stream of nitrogen using blow down apparatus. Purification by mass directed preparative HPLC (Method C) gave the title compound.

後処理

  1. waitThe reaction mixture was left
  2. waitto stand at 22° C. for 18 h
  3. customThe solvent was removed in vacuo
  4. dissolutionthe product re-dissolved in chloroform (0.3 ml)
  5. washThe product was eluted after 2 hr with ethyl acetate/methanol (1:1, 3 ml)
  6. concentrationconcentrated under a stream of nitrogen using blow down apparatus
  7. customPurification by mass

出典と根拠

ORDレコード
ord-030c54546ca744bd89c0909c47ab224a
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08658635B2

反応ノート

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