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Ammonium Chloride → HCID 86664655、化合物

HRID 1917404
ノート
印刷プレビュー

反応式

HRID 1917404 の反応式
[CH2:1]1CCN2C(=NCCC2)CC1.C[N+](C)=C.[I-].[C:17]([O:21][C:22]([C@@:24]1([CH2:38][CH2:39][CH:40]=[O:41])[CH2:28][C:27](=[O:29])[N:26]([C@@H:30]([C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[CH3:31])[CH2:25]1)=[O:23])([CH3:20])([CH3:19])[CH3:18].[Cl-].[NH4+]>ClCCl>[C:17]([O:21][C:22]([C@@:24]1([CH2:38][C:39](=[CH2:1])[CH:40]=[O:41])[CH2:28][C:27](=[O:29])[N:26]([C@@H:30]([C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[CH3:31])[CH2:25]1)=[O:23])([CH3:20])([CH3:19])[CH3:18]
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 4

HCID 25517Ammonium ChlorideHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 2724133Dimethyl(methylene)ammounium iodide2 回HCID 86664654(3S)-3-(3-Oxo-1-propyl)-5-oxo-1-[(1R)-1-phenylethyl]pyrrolidine-3-carboxylic acid tert-butyl ester

生成物 1

HCID 86664655HCID 86664655、化合物

試薬・触媒・溶媒 1

HCID 6344
Dichloromethane
溶媒

実験手順

1,8-Diazabicyclo[5.4.0]-7-undecene (2.17 ml, 14.5 mmol) and Eschenmoser salt (3.66 g, 19.8 mmol) were added to a solution of (3S)-3-(3-oxo-1-propyl)-5-oxo-1-[(1R)-1-phenylethyl]pyrrolidine-3-carboxylic acid tert-butyl ester in dichloromethane (88.0 ml) in a nitrogen atmosphere, and the mixture was stirred at room temperature for 16 hours. Thereafter, Eschenmoser salt (1.22 g, 6.59 mmol) was added, and the mixture was stirred at room temperature for three hours. A saturated ammonium chloride solution (150 ml) was added to the reaction solution, followed by extraction with chloroform (100 ml×1, 150 ml×1). The organic layer was washed with brine (200 ml) and then dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=100:0→90:10→66:34→60:40→50:50→34:66) to give 3.14 g of the title compound as white crystals.

後処理

  1. stirringthe mixture was stirred at room temperature for three hours
  2. extractionfollowed by extraction with chloroform (100 ml×1, 150 ml×1)
  3. washThe organic layer was washed with brine (200 ml)
  4. dry with materialdried over anhydrous sodium sulfate
  5. filtrationAfter filtration
  6. concentrationthe filtrate was concentrated under reduced pressure
  7. customThe resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=100:0→90:10→66:34→60:40→50:50→34:66)

出典と根拠

ORDレコード
ord-f7aa2a94ed394d919730325a1a8514cc
出典データセット
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08618094B2

反応ノート

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