ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Acetonitrile → (2S,4S)-4-(4-Methoxybenzylthio)-2-(4-t-butoxy-carbonyl-2-methylpiperazin-1-ylcarbonyl)-1-(4-nitro-benzyloxycarbonyl)pyrrolidine

HRID 362022
ノート
印刷プレビュー

反応式

HRID 362022 の反応式
C([N:3]([CH2:6][CH3:7])[CH2:4][CH3:5])C.[C:8](Cl)(=[O:13])[C:9](C)(C)C.[CH3:15][O:16][C:17]1[CH:45]=[CH:44][C:20]([CH2:21][S:22][C@@H:23]2[CH2:27][N:26]([C:28]([O:30][CH2:31][C:32]3[CH:37]=[CH:36][C:35]([N+:38]([O-:40])=[O:39])=[CH:34][CH:33]=3)=[O:29])[C@H:25]([C:41](O)=[O:42])[CH2:24]2)=[CH:19][CH:18]=1.[C:46]([O:50]C(N1CCNC(C)C1)=O)([CH3:49])([CH3:48])[CH3:47].C(#[N:62])C>O1CCCC1>[CH3:15][O:16][C:17]1[CH:45]=[CH:44][C:20]([CH2:21][S:22][C@@H:23]2[CH2:27][N:26]([C:28]([O:30][CH2:31][C:32]3[CH:33]=[CH:34][C:35]([N+:38]([O-:40])=[O:39])=[CH:36][CH:37]=3)=[O:29])[C@H:25]([C:41]([N:3]3[CH2:4][CH2:5][N:62]([O:50][C:46]([CH3:47])([CH3:48])[CH3:49])[C:9](=[C:8]=[O:13])[CH:6]3[CH3:7])=[O:42])[CH2:24]2)=[CH:19][CH:18]=1
参加物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 6342AcetonitrileHCID 8471TriethylamineHCID 62493Pivaloyl chlorideHCID 2756810tert-Butyl 3-methylpiperazine-1-carboxylateHCID 15297071(2S,4S)-4-(4-methoxybenzyl)thio-1-(4-nitrobenzyloxycarbonyl)-L-proline

生成物 1

HCID 86753693
(2S,4S)-4-(4-Methoxybenzylthio)-2-(4-t-butoxy-carbonyl-2-methylpiperazin-1-ylcarbonyl)-1-(4-nitro-benzyloxycarbonyl)pyrrolidine

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

3.41 ml of triethylamine and 3.03 ml of pivaloyl chloride were added dropwise to a solution of 9.99 g of (2S,4S)-4-(4-methoxybenzylthio)-1-(4-nitrobenzyloxy-carbonyl)-2-pyrrolidinecarboxylic acid in 100 ml of dry acetonitrile, whilst ice-cooling, and the resulting mixture was stirred at the same temperature for 20 minutes. A solution of 5.38 g of 1-t-butoxycarbonyl-3-methylpiperazine in 50 ml of dry tetrahydrofuran was then added dropwise to the mixture, and the mixture was stirred at the same temperature for 30 minutes and then at room temperature for 2 hours. At the end of this time, the reaction mixture was concentrated by evaporation under reduced pressure, and the residue was diluted with ethyl acetate. The diluted solution was washed, in turn, with a 1N aqueous solution of oxalic acid, with water and with an aqueous solution of sodium chloride. The ethyl acetate solution was dried over anhydrous magnesium sulfate, and the solvent was removed by distillation under reduced pressure. The residue was purified by column chromatography through silica gel, using a gradient elution method, with mixtures of ethyl acetate and cyclcohexane ranging from 1:1 to 3:2 by volume as the eluent, to give 8.56 g of the title compound, as an amorphous solid.

後処理

  1. temperaturecooling
  2. stirringthe mixture was stirred at the same temperature for 30 minutes
  3. waitat room temperature for 2 hours
  4. concentrationAt the end of this time, the reaction mixture was concentrated by evaporation under reduced pressure
  5. additionthe residue was diluted with ethyl acetate
  6. washThe diluted solution was washed, in turn, with a 1N aqueous solution of oxalic acid, with water and with an aqueous solution of sodium chloride
  7. dry with materialThe ethyl acetate solution was dried over anhydrous magnesium sulfate
  8. customthe solvent was removed by distillation under reduced pressure
  9. customThe residue was purified by column chromatography through silica gel
  10. washa gradient elution method

出典と根拠

ORDレコード
ord-7ed6c3ed58354b609bdc5ea99e1c6550
出典データセット
uspto-grants-1999_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05866564

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