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Morpholine → (1-Benzyl-3-bromo-4-methyl-5-(trifluoromethyl)-1H-pyrrol-2-yl)(morpholino)methanone

HRID 623789
ノート
印刷プレビュー

反応式

HRID 623789 の反応式
CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C.[CH2:34]([N:41]1[C:45]([C:46]([F:49])([F:48])[F:47])=[C:44]([CH3:50])[C:43]([Br:51])=[C:42]1[C:52]([OH:54])=O)[C:35]1[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1.[NH:55]1[CH2:60][CH2:59][O:58][CH2:57][CH2:56]1>CN(C=O)C.CCOC(C)=O.O>[CH2:34]([N:41]1[C:45]([C:46]([F:47])([F:48])[F:49])=[C:44]([CH3:50])[C:43]([Br:51])=[C:42]1[C:52]([N:55]1[CH2:60][CH2:59][O:58][CH2:57][CH2:56]1)=[O:54])[C:35]1[CH:36]=[CH:37][CH:38]=[CH:39][CH:40]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 8083MorpholineHCID 81531DiisopropylethylamineHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 867118651-Benzyl-3-bromo-4-methyl-5-(trifluoromethyl)-1H-pyrrole-2-carboxylic acid

生成物 1

HCID 86711874(1-Benzyl-3-bromo-4-methyl-5-(trifluoromethyl)-1H-pyrrol-2-yl)(morpholino)methanone
収率 84%

試薬・触媒・溶媒 3

HCID 962Water溶媒HCID 6228Dimethylformamide溶媒HCID 8857Ethyl Acetate溶媒

実験手順

HATU (12.59 g 33.14 mmol) and DIPEA (12.3 mL, 33.14 mmol) were added to the ice cold solution of 1-benzyl-3-bromo-4-methyl-5-(trifluoromethyl)-1H-pyrrole-2-carboxylic acid (10 g, 27.62 mmol) in DMF (110 mL) and it was stirred for 10 min at same temperature and then morpholine (2.8 mL, 33.14 mmol) was added to the reaction mixture warmed to RT and then stirred for 14 h. The reaction mixture was diluted with EtOAc and H2O. The aqueous layer was extracted with EtOAc (2×300 mL), washed with water (2×300 mL) and brine (2×300 mL), organic layer was dried over anhydrous Na2SO4, combined organic layer was dried over anhydrous Na2SO4 and concentrated under reduced pressure to yield crude mass which was then purified by column chromatography (100-200 mesh Silica gel; 30% ethyl acetate/hexane; Rf-value 0.6) to afford title compound (10 g, 84% yield, white color solid).

後処理

  1. stirringstirred for 14 h
  2. extractionThe aqueous layer was extracted with EtOAc (2×300 mL)
  3. washwashed with water (2×300 mL) and brine (2×300 mL), organic layer
  4. dry with materialwas dried over anhydrous Na2SO4
  5. dry with materialwas dried over anhydrous Na2SO4
  6. concentrationconcentrated under reduced pressure
  7. customto yield crude mass which
  8. customwas then purified by column chromatography (100-200 mesh Silica gel; 30% ethyl acetate/hexane; Rf-value 0.6)

出典と根拠

ORDレコード
ord-76a414e6f0474300864a3ee493e0cf6e
出典データセット
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09302988B2

反応ノート

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