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Triethylamine → HCID 70559499、化合物

HRID 2052095
ノート
印刷プレビュー

反応式

HRID 2052095 の反応式
C(N(CC)CC)C.[Br:8]N1C(=O)CCC1=O.[C:16]([NH:24][CH:25]1[C:41](=[O:42])[N:27]2[C:28]([C:34]([O:36][C:37]([CH3:40])([CH3:39])[CH3:38])=[O:35])=[C:29]([CH3:33])[CH2:30][S:31](=[O:32])[C@H:26]12)(=[O:23])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>C(Cl)Cl.[W]>[C:16]([NH:24][CH:25]1[C:41](=[O:42])[N:27]2[C:28]([C:34]([O:36][C:37]([CH3:38])([CH3:40])[CH3:39])=[O:35])=[C:29]([CH3:33])[CH:30]([Br:8])[S:31](=[O:32])[C@H:26]12)(=[O:23])[C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 8471TriethylamineHCID 67184N-bromobutanimideHCID 70464442t-Butyl 7-benzamido-3-methyl-3-cephem-4-carboxylate 1-oxide

生成物 1

HCID 70559499HCID 70559499、化合物収率 112.9%

試薬・触媒・溶媒 2

HCID 23964Tungsten触媒HCID 6344Dichloromethane
溶媒

実験手順

4.2 ml (30 mmoles) of triethylamine and 3.28 g (24 mmoles) of N-bromosuccinimide were sequentially added to a solution of 7.8 g (20 mmoles) of t-butyl 7-benzamido-3-methyl-3-cephem-4-carboxylate 1-oxide in 150 ml of methylene chloride under nitrogen and cooled in an ice bath and the mixture was irradiated with a 150 W tungsten lamp for 15 minutes. The dark-brown reaction mixture was washed with a dilute hydrochloric acid solution (pH 1) and then twice with 250 ml portions of water. The organic layer was dried over magnesium sulfate, filtered and evaporated to dryness to obtain 10.6 g (70% yield-purity 62%) of t-butyl 7-benzamido-2-bromo-3-methyl-3-cephem-4-carboxylate 1-oxide.

後処理

  1. temperaturecooled in an ice bath
  2. washThe dark-brown reaction mixture was washed with a dilute hydrochloric acid solution (pH 1)
  3. dry with materialThe organic layer was dried over magnesium sulfate
  4. filtrationfiltered
  5. customevaporated to dryness

出典と根拠

ORDレコード
ord-172a2682708944fbb0ea44b360c7bd74
出典データセット
uspto-grants-1980_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04182870

反応ノート

読み込み中…

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