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
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
- temperatureby heating
- temperatureThe resulting mixture was heated
- temperatureunder reflux for 2 h
- filtrationThe hot reaction mixture was filtered
- additionthe filtrate was treated with aqueous 2M NaOH (560 mL)
- filtrationfiltered again
- washThe filter cake was washed with methanol
- customThe methanol was removed under reduced pressure
- extractionthe aqueous mixture was extracted three times with ethyl acetate
- washThe organic solution was washed with water and brine
- dry with materialdried with magnesium sulfate
- filtrationfiltered
- customevaporated to dryness
- customIt was obtained a yellowish crystalline material with the yield of 4.62 g
- customRecrystallisation from the dichlomethane-methanol mixture
- 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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