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4-Methylmorpholine → HCID 178454356、化合物

HRID 2051590
ノート
印刷プレビュー

反応式

HRID 2051590 の反応式
C(CC(O)=O)C.[C:7]([N:14]([C:25]([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:26])[C@H:15]([C:22](O)=[O:23])[CH2:16][C:17]1[N:21]=[CH:20][NH:19][CH:18]=1)([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8].C[N:33]1CCOCC1.ClC(OCC(C)C)=O.C(OC[C@@H](N)CC(C)C)C>C(OCC)(=O)C>[C:7]([N:14]([C:25]([O:27][C:28]([CH3:31])([CH3:29])[CH3:30])=[O:26])[C@H:15]([C:22]([NH2:33])=[O:23])[CH2:16][C:17]1[N:21]=[CH:20][NH:19][CH:18]=1)([O:9][C:10]([CH3:11])([CH3:13])[CH3:12])=[O:8]
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 79724-MethylmorpholineHCID 62365Isobutyl chloroformateHCID 15745497HCID 15745497、化合物HCID 178454358HCID 178454358、化合物

生成物 1

HCID 178454356HCID 178454356、化合物

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒2 回

実験手順

A mixture of Nα -Nim -bis-BOC-histidine ethyl acetate solvale (1.92 g, 5.0 mmol), 4-methylmorpholine (0.55 mL, 5.0 mmol) and isobutyl chloroformate (0.65 mL, 5.0 mmol) in ethyl acetate (50 mL) was stirred in an ice bath under N2 for 15 minutes. A solution of (S)-1-ethoxy-2-amino-4-methylpentane (0.73 g, 5.0 mmol) in ethyl acetate (2 mL) was then added and the reaction stirred at room temperature for 20 hours. After washing with 10% citric acid, brine, saturated NaHCO3 solution and brine, the ethyl acetate extract was dried (Na2SO4), filtered and concentrated under reduced pressure. The residue was flash chromatographed over silica gel. Elution with a mixture of 2% methanol and 98% chloroform afforded pure BOC-protected histidineamide (0.90 g).

後処理

  1. stirringthe reaction stirred at room temperature for 20 hours
  2. washAfter washing with 10% citric acid, brine, saturated NaHCO3 solution and brine
  3. extractionthe ethyl acetate extract
  4. dry with materialwas dried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customchromatographed over silica gel
  8. washElution
  9. additionwith a mixture of 2% methanol and 98% chloroform afforded pure BOC-protected histidineamide (0.90 g)

出典と根拠

ORDレコード
ord-1ff0c6a80f154f1a8a86bfcd3dd296af
出典データセット
uspto-grants-1991_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05019647

反応ノート

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