Hydrochloric Acid → HCID 9815456, 화합물

HRID 1096492

반응식

HRID 1096492 반응식
[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

참가 물질

5

실험 절차

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]+.

후처리

  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

출처 및 근거

ORD 기록
ord-a4f9c55ab03846fb87f2ecb69505f810
출처 데이터셋
uspto-grants-2012_03
특허 번호
US08138333B2

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