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氨 → HCID 68584641,化合物

HRID 17544
笔记
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反应方程式

HRID 17544 反应方程式
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
参与物实验过程后处理来源与证据反应笔记

参与物

6

反应物 4

HCID 222氨HCID 27239391-乙基-(3-二甲基氨基丙基)碳酰二亚胺盐酸盐HCID 685849474-Bromo-2-tert-butyl-5-phenyl-1-benzofuran-7-carboxylic AcidHCID 178418300HCID 178418300,化合物

产物 1

HCID 68584641HCID 68584641,化合物收率 99.1%

试剂、催化剂与溶剂 1

HCID 6228N,N-二甲基甲酰胺
溶剂

实验过程

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.

后处理

  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)

来源与证据

ORD记录
ord-eae3def2b7324364bd8d651b14d92b4f
来源数据集
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
专利号
US07737166B2

反应笔记

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本页导航参与物实验过程后处理来源与证据反应笔记