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Bis(2-Methoxyethyl)amine → (S)-8-chloro-1-[5-di(2-methoxyethyl)aminomethyl-1,2,4-oxadiazol-3-yl]-12,12a-dihydro-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepin-9-one

HRID 1378183
ノート
印刷プレビュー

反応式

HRID 1378183 の反応式
[Cl:1][C:2]1[C:7]2[C:8](=[O:25])[N:9]3[CH2:24][CH2:23][C@H:10]3[C:11]3[N:12]([CH:13]=[N:14][C:15]=3[C:16]3[N:20]=[C:19]([CH2:21]Cl)[O:18][N:17]=3)[C:6]=2[CH:5]=[CH:4][CH:3]=1.[CH3:26][O:27][CH2:28][CH2:29][NH:30][CH2:31][CH2:32][O:33][CH3:34]>CN(C)C=O>[Cl:1][C:2]1[C:7]2[C:8](=[O:25])[N:9]3[CH2:24][CH2:23][C@H:10]3[C:11]3[N:12]([CH:13]=[N:14][C:15]=3[C:16]3[N:20]=[C:19]([CH2:21][N:30]([CH2:31][CH2:32][O:33][CH3:34])[CH2:29][CH2:28][O:27][CH3:26])[O:18][N:17]=3)[C:6]=2[CH:5]=[CH:4][CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 2383Bis(2-Methoxyethyl)amineHCID 53954665(S)-8-chloro-1-(5-chloromethyl-1,2,4-oxadiazol-3-yl)-12,12a-dihydro-9H,11H-azeto[2,1-c]-imidazo[1,5-a][1,4]benzodiazepin-9-one

生成物 1

HCID 53839106(S)-8-chloro-1-[5-di(2-methoxyethyl)aminomethyl-1,2,4-oxadiazol-3-yl]-12,12a-dihydro-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepin-9-one収率 211.5%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

1.88 g (5 mmol) of (S)-8-chloro-1-(5-chloromethyl-1,2,4-oxadiazol-3-yl)-12,12a-dihydro-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepin-9-one were stirred at room temperature for 4 hours with 2 g (2.2 mmol) of bis(2-methoxyethyl)-amine and 15 ml of N,N-dimethylformamide. After evaporating the solvent the reaction mixture was taken up in 4N sodium hydroxide solution, whereupon the mixture was extracted three times with methylene chloride. By drying the organic phase over magnesium sulfate and evaporating the solvent there were obtained 2.2 g (93%) of (S)-8-chloro-1-[5-di(2-methoxyethyl)aminomethyl-1,2,4-oxadiazol-3-yl]-12,12a-dihydro-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepin-9-one, which was converted into the hydrochloride of m.p. 188°-190°.

後処理

  1. customAfter evaporating the solvent the reaction mixture
  2. extractionwas extracted three times with methylene chloride
  3. dry with materialBy drying the organic phase over magnesium sulfate
  4. customevaporating the solvent there

出典と根拠

ORDレコード
ord-5ebc305f18d34007ab73dfc35534bf60
出典データセット
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05665718

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート