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Ammonium Chloride → HCID 67976218、化合物

HRID 706670
ノート
印刷プレビュー

反応式

HRID 706670 の反応式
I[C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][C:9]=2[N+:11]([O-])=O)[N:4]([CH2:14][C:15]2[CH:16]=[C:17]([CH:22]=[CH:23][CH:24]=2)[C:18]([O:20][CH3:21])=[O:19])[N:3]=1.[NH4+].[Cl-]>CO.[Zn]>[NH2:11][C:9]1[CH:8]=[CH:7][CH:6]=[C:5]2[C:10]=1[CH:2]=[N:3][N:4]2[CH2:14][C:15]1[CH:16]=[C:17]([CH:22]=[CH:23][CH:24]=1)[C:18]([O:20][CH3:21])=[O:19]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 25517Ammonium ChlorideHCID 67976101Methyl 3-((3-iodo-4-nitro-1H-indazol-1-yl)methyl)benzoate

生成物 1

HCID 67976218HCID 67976218、化合物収率 61.8%

試薬・触媒・溶媒 2

HCID 23994Zinc触媒HCID 887Methanol溶媒2 回

反応条件

温度
0 °C

実験手順

A suspension of methyl 3-((3-iodo-4-nitro-1H-indazol-1-yl)methyl)benzoate (1.00 g, 2.29 mmol) and MeOH (45 mL) was cooled to 0° C. Zinc dust (0.748 g, 11.4 mmol) was added followed by saturated aqueous NH4Cl (23 mL). The mixture was stirred at 0° C. for 2 hours, then warmed to ambient temperature and stirred for an additional 3 hours. The mixture was diluted with MeOH and filtered. To the filtrate was added saturated aqueous NH4OAc and the mixture was concentrated to remove bulk MeOH. The concentrated mixture was extracted with EtOAc and the combined organic extracts were washed with saturated aqueous NaHCO3 and brine, then dried over Na2SO4, filtered and concentrated. The product was purified by column chromatography (25 to 100% EtOAc/hexane) to afford 0.398 g (61%) of the title compound as a sticky orange foam.

後処理

  1. temperaturewarmed to ambient temperature
  2. stirringstirred for an additional 3 hours
  3. filtrationfiltered
  4. additionTo the filtrate was added saturated aqueous NH4OAc
  5. concentrationthe mixture was concentrated
  6. customto remove bulk MeOH
  7. extractionThe concentrated mixture was extracted with EtOAc
  8. washthe combined organic extracts were washed with saturated aqueous NaHCO3 and brine
  9. dry with materialdried over Na2SO4
  10. filtrationfiltered
  11. concentrationconcentrated
  12. customThe product was purified by column chromatography (25 to 100% EtOAc/hexane)

出典と根拠

ORDレコード
ord-50fa0481bf784ac4858f6a48a615bf9f
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09174981B2

反応ノート

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