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1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 22122152、化合物

HRID 1859175
ノート
印刷プレビュー

反応式

HRID 1859175 の反応式
[N:1]([CH2:4][CH2:5][N:6]1[CH2:11][CH2:10][NH:9][C:8](=[O:12])[C:7]1=[O:13])=[N+:2]=[N-:3].[N:14]1[CH:19]=[CH:18][CH:17]=[C:16]([CH:20]=[CH:21][C:22]([O:24][CH:25]([C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)=[O:23])[CH:15]=1.N12CCCN=C1CCCCC2>CN(C)C=O>[N:1]([CH2:4][CH2:5][N:6]1[CH2:11][CH2:10][N:9]([CH:20]([C:16]2[CH:15]=[N:14][CH:19]=[CH:18][CH:17]=2)[CH2:21][C:22]([O:24][CH:25]([C:26]2[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=2)[C:32]2[CH:33]=[CH:34][CH:35]=[CH:36][CH:37]=2)=[O:23])[C:8](=[O:12])[C:7]1=[O:13])=[N+:2]=[N-:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 22122160HCID 22122160、化合物HCID 54425842HCID 54425842、化合物

生成物 1

HCID 22122152HCID 22122152、化合物収率 52.2%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

A mixture of 0.5 g of 1-(2-azidoethyl)-2,3-dioxopiperazine, 1.72 g of diphenylmethyl 3-(3-pyridyl)-acrylate, 0.2 ml of 1,8-diazabicyclo[5.4.0]undec-7-ene and 2.5 ml of N,N-dimethylformamide was stirred at room temperature for 12 hours. The solvent was distilled off under reduced pressure, after which 30 ml of ethyl acetate and 20 ml of water were added to the resulting residue and the pH was adjusted to 6 with 2N hydrochloric acid. The organic layer was separated and the aqueous layer was extracted with 30 ml of ethyl acetate. The combined organic layer was washed with 20 ml of water and a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was purified by a silica gel column chromatography (eluent; chloroform:methanol=20:1) to obtain 0.71 g of diphenylmethyl 3-[4-(2-azidoethyl)-2,3-dioxopiperazin-1-yl]-3-(pyridin-3-yl)propionate as a light-brown oil.

後処理

  1. distillationThe solvent was distilled off under reduced pressure
  2. additionafter which 30 ml of ethyl acetate and 20 ml of water were added to the resulting residue
  3. customThe organic layer was separated
  4. extractionthe aqueous layer was extracted with 30 ml of ethyl acetate
  5. washThe combined organic layer was washed with 20 ml of water
  6. dry with materiala saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate
  7. distillationThe solvent was distilled off under reduced pressure
  8. customthe resulting residue was purified by a silica gel column chromatography (eluent; chloroform:methanol=20:1)

出典と根拠

ORDレコード
ord-58378ebd76e4428ab27293aa489c4e81
出典データセット
uspto-grants-2000_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06153613

反応ノート

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