Hydrochloric Acid → Ethyl 3-chloro-6-nitroindazol-1-ylacetate

HRID 1464576

反応式

HRID 1464576 の反応式
[Cl:1][C:2]1[C:10]2[C:5](=[CH:6][C:7]([N+:11]([O-:13])=[O:12])=[CH:8][CH:9]=2)[NH:4][N:3]=1.[H-].[Na+].Br[CH2:17][C:18]([O:20][CH2:21][CH3:22])=[O:19].Cl>CN(C=O)C.C(OCC)(=O)C.O>[Cl:1][C:2]1[C:10]2[C:5](=[CH:6][C:7]([N+:11]([O-:13])=[O:12])=[CH:8][CH:9]=2)[N:4]([CH2:17][C:18]([O:20][CH2:21][CH3:22])=[O:19])[N:3]=1

参加物

8

反応物 4

HCID 313Hydrochloric AcidHCID 7748Ethyl bromoacetateHCID 24758Sodium hydrideHCID 178526457HCID 178526457、化合物

生成物 1

HCID 19086706Ethyl 3-chloro-6-nitroindazol-1-ylacetate収率 56.6%

試薬・触媒・溶媒 3

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

反応条件

温度
5 °C

実験手順

3-chloro-6-nitroindazole (20 g) was dissolved in dry DMF (180cm3) and the solution cooled to 5° C. 50% sodium hydride (4.86 g) was added portionwise with stirring and cooling between 5° and 10° C. and then for an additional 15 minutes. Ethyl bromoacetate (16.91 g) was added slowly at 5° C., the reaction mixture warming to 30° C. The reaction mixture was then stirred at 20° C. for four hours. Water (lL) was added and the mixture acidified with diluted hydrochloric acid, shaken with ethyl acetate and filtered through hyflo. The organic phase was separated from the filtrate and the aqueous phase extracted (×2) with ethyl acetate. The combined organic phase was washed with water, dried (MgSO4) filtered and the solvent removed from the filtrate under vacuum. The residue was purified by flash chromatography (SiO2 ; hexane: TBME, 7:3 and then chloroform:ethyl acetate 95:5) to give ethyl 3-chloro-6-nitroindazol-1-ylacetate (16.25 g) as a pale yellow solid m.pt 109.1°-110.3° C.

後処理

  1. temperaturecooling between 5° and 10° C.
  2. temperaturethe reaction mixture warming to 30° C
  3. stirringThe reaction mixture was then stirred at 20° C. for four hours
  4. filtrationfiltered through hyflo
  5. customThe organic phase was separated from the filtrate
  6. extractionthe aqueous phase extracted (×2) with ethyl acetate
  7. washThe combined organic phase was washed with water
  8. dry with materialdried (MgSO4)
  9. filtrationfiltered
  10. customthe solvent removed from the filtrate under vacuum
  11. customThe residue was purified by flash chromatography (SiO2

出典と根拠

ORDレコード
ord-afbdf5edbd7e49f1a8c3810ab5fc418a
出典データセット
uspto-grants-1994_04
特許番号
US05306692

関連ノート

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