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Ammonium Hydroxide → 2-[2-(3,5-dimethylphenyl)-3-[2-[4-(pyridin-4-yl)butylamino]ethyl]-1H-indol-5-yl]-N,N-diethylisobutyramide

HRID 1458354
ノート
印刷プレビュー

反応式

HRID 1458354 の反応式
[NH2:1][CH2:2][CH2:3][C:4]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([C:13]([CH3:22])([CH3:21])[C:14]([N:16]([CH2:19][CH3:20])[CH2:17][CH3:18])=[O:15])[CH:11]=2)[NH:6][C:5]=1[C:23]1[CH:28]=[C:27]([CH3:29])[CH:26]=[C:25]([CH3:30])[CH:24]=1.[N:31]1[CH:36]=[CH:35][C:34]([CH2:37][CH2:38][CH2:39][CH:40]=O)=[CH:33][CH:32]=1.S([O-])([O-])(=O)=O.[Mg+2].[BH4-].[Na+].[NH4+].[OH-]>CO>[CH3:30][C:25]1[CH:24]=[C:23]([C:5]2[NH:6][C:7]3[C:12]([C:4]=2[CH2:3][CH2:2][NH:1][CH2:40][CH2:39][CH2:38][CH2:37][C:34]2[CH:35]=[CH:36][N:31]=[CH:32][CH:33]=2)=[CH:11][C:10]([C:13]([CH3:22])([CH3:21])[C:14]([N:16]([CH2:19][CH3:20])[CH2:17][CH3:18])=[O:15])=[CH:9][CH:8]=3)[CH:28]=[C:27]([CH3:29])[CH:26]=1
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

7

反応物 5

HCID 14923Ammonium HydroxideHCID 24083Sulfuric acid magnesium salt (1:1)HCID 4311764Sodium borohydrideHCID 114464344-Pyridin-4-ylbutanalHCID 121499922-[3-(2-aminoethyl)-2-(3,5-dimethylphenyl)-1H-indol-5-yl]-N,N-diethylisobutyramide

生成物 1

HCID 22100905
2-[2-(3,5-dimethylphenyl)-3-[2-[4-(pyridin-4-yl)butylamino]ethyl]-1H-indol-5-yl]-N,N-diethylisobutyramide

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
-10 °C

実験手順

A mixture of 93.3 mg (0.23 mmol) of 2-[3-(2-aminoethyl)-2-(3,5-dimethylphenyl)-1H-indol-5-yl]-N,N-diethylisobutyramide, 37.7 mg (0.253 mmol) of 4-(pyridin-4-yl)butyraldehyde, and 138 mg (1.15 mmol) of magnesium sulfate was purged with nitrogen and cooled in an ice-methanol bath at about -10° C. as 0.50 mL of CDCl3 was added gradually by syringe. The mixture was stirred under nitrogen at this temperature for 1 hour. The septum was removed just long enough to add 11.3 mg (0.30 mmol) of sodium borohydride, and the solution was repurged with nitrogen. The mixture was stirred at -10° to -5° C. as 0.50 mL of dry methanol was added gradually, and stirring was continued at this temperature. After 35 minutes, the mixture was partitioned between 5 mL of ethyl acetate and 5 mL of water. The ethyl acetate layer was washed with brine, then dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by two stages of preparative TLC on Analtech tapered silica gel GF plates (developed first in 90:10:1 methylene chloride -methanol-ammonium hydroxide and repeated in 90:10 methylene chloride -methanol). Isolation of the product bands gave 25.7 mg (21%) of light golden-colored glassy residue; virtually homogenous by TLC in 92.5:7.5:0.75 CH2Cl2 -MeOH-concd. NH4OH. 500 MHz 1H NMR (CDCl3) was consistent with the assigned structure. Mass spectrum (ESI): m/e=539 (M+H).

後処理

  1. customwas purged with nitrogen
  2. additionwas added gradually by syringe
  3. customThe septum was removed just long enough
  4. additionwas added gradually
  5. stirringstirring
  6. waitAfter 35 minutes
  7. customthe mixture was partitioned between 5 mL of ethyl acetate and 5 mL of water
  8. washThe ethyl acetate layer was washed with brine
  9. dry with materialdried over sodium sulfate
  10. filtrationfiltered
  11. concentrationconcentrated in vacuo
  12. customThe residue was purified by two stages of preparative TLC on Analtech
  13. customIsolation of the product bands gave 25.7 mg (21%) of light golden-colored glassy residue

出典と根拠

ORDレコード
ord-3fea8f5795ab42bb9587474b1a00f853
出典データセット
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05849764

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート