Hydrochloric Acid → HCID 9815456、化合物

HRID 1096492

反応式

HRID 1096492 の反応式
[N+:1]([CH2:4][CH2:5][C:6]1[C:14]2[C:13]([C:15]([O:17]C)=O)=[CH:12][CH:11]=[CH:10][C:9]=2[NH:8][CH:7]=1)([O-])=O.Cl>CO.[Zn]>[NH:8]1[C:9]2[CH:10]=[CH:11][CH:12]=[C:13]3[C:15](=[O:17])[NH:1][CH2:4][CH2:5][C:6]([C:14]=23)=[CH:7]1

参加物

5

実験手順

Methyl 3-(2-nitroethyl)-1H-indole-4-carboxylate, Intermediate 9 (7.38 g, 29.8 mmol) was dissolved in methanol (200 mL) by heating and aqueous 2M HCl (460 mL) was added. Zinc powder (46.2 g, 706 mmol) was added portion vise by vigorous stirring. The resulting mixture was heated under reflux for 2 h. The hot reaction mixture was filtered and the filtrate was treated with aqueous 2M NaOH (560 mL) and filtered again. The filter cake was washed with methanol. The methanol was removed under reduced pressure and the aqueous mixture was extracted three times with ethyl acetate. The organic solution was washed with water and brine dried with magnesium sulfate, filtered and evaporated to dryness. It was obtained a yellowish crystalline material with the yield of 4.62 g. Recrystallisation from the dichlomethane-methanol mixture gave the product of very high purity. Mp. 234° C. MS m/z 187 [M+H]+.

後処理

  1. temperatureby heating
  2. temperatureThe resulting mixture was heated
  3. temperatureunder reflux for 2 h
  4. filtrationThe hot reaction mixture was filtered
  5. additionthe filtrate was treated with aqueous 2M NaOH (560 mL)
  6. filtrationfiltered again
  7. washThe filter cake was washed with methanol
  8. customThe methanol was removed under reduced pressure
  9. extractionthe aqueous mixture was extracted three times with ethyl acetate
  10. washThe organic solution was washed with water and brine
  11. dry with materialdried with magnesium sulfate
  12. filtrationfiltered
  13. customevaporated to dryness
  14. customIt was obtained a yellowish crystalline material with the yield of 4.62 g
  15. customRecrystallisation from the dichlomethane-methanol mixture
  16. customgave the product of very high purity

出典と根拠

ORDレコード
ord-a4f9c55ab03846fb87f2ecb69505f810
出典データセット
uspto-grants-2012_03
特許番号
US08138333B2

関連ノート

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