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Ammonia → HCID 68584641、化合物

HRID 17544
ノート
印刷プレビュー

反応式

HRID 17544 の反応式
Cl.C([N:4]=C=NCCCN(C)C)C.[Br:13][C:14]1[C:19]2[CH:20]=[C:21]([C:23]([CH3:26])([CH3:25])[CH3:24])[O:22][C:18]=2[C:17]([C:27](O)=[O:28])=[CH:16][C:15]=1[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1.OC1C2N=NNC=2C=CC=1.N>CN(C)C=O>[Br:13][C:14]1[C:19]2[CH:20]=[C:21]([C:23]([CH3:26])([CH3:25])[CH3:24])[O:22][C:18]=2[C:17]([C:27]([NH2:4])=[O:28])=[CH:16][C:15]=1[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=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 222AmmoniaHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 685849474-Bromo-2-tert-butyl-5-phenyl-1-benzofuran-7-carboxylic AcidHCID 178418300HCID 178418300、化合物

生成物 1

HCID 68584641HCID 68584641、化合物収率 99.1%

試薬・触媒・溶媒 1

HCID 6228
Dimethylformamide
溶媒

実験手順

1-Ethyl-3-[3-(dimethylamino)propyl]carbodiimide hydrochloride (1.61 g, 8.42 mmol) was added to an N,N-dimethylformamide (80 ml) solution of 4-bromo-2-tert-butyl-5-phenyl-1-benzofuran-7-carboxylic acid (I-256) (2.62 g, 7.02 mmol) and hydroxybenzotriazole (1.14 g, 8.42 mmol), followed by stirring at room temperature for 1 hour. The reaction liquid was cooled at 0° C., then aqueous 28% ammonia (1.42 ml, 21.1 mmol) was put into it, followed by further stirring at room temperature for 1 hour. The reaction liquid was concentrated under reduced pressure, then saturated sodium bicarbonate water (200 ml) was added, the product was extracted with ethyl acetate (200 ml×2). The organic layer was washed with saturated brine (50 ml), then dried over anhydrous magnesium sulfate, concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=3:2) to obtain the entitled compound (2.59 g, 99%) as a yellow white solid.

後処理

  1. customThe reaction liquid
  2. temperaturewas cooled at 0° C.
  3. stirringby further stirring at room temperature for 1 hour
  4. customThe reaction liquid
  5. concentrationwas concentrated under reduced pressure
  6. additionsaturated sodium bicarbonate water (200 ml) was added
  7. extractionthe product was extracted with ethyl acetate (200 ml×2)
  8. washThe organic layer was washed with saturated brine (50 ml)
  9. dry with materialdried over anhydrous magnesium sulfate
  10. concentrationconcentrated under reduced pressure
  11. customthe residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=3:2)

出典と根拠

ORDレコード
ord-eae3def2b7324364bd8d651b14d92b4f
出典データセット
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07737166B2

反応ノート

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