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HCID 131726535, 화합물 → HCID 131726536, 화합물

HRID 1159075
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HRID 1159075 반응식
C(OC([NH:8][C@@:9]([CH3:26])([C:17]([NH:19][CH2:20][C:21]([O:23][CH2:24][CH3:25])=[O:22])=[O:18])[CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=O)(C)(C)C>Cl.O1CCOCC1>[CH3:26][C@:9]([C:17]([NH:19][CH2:20][C:21]([O:23][CH2:24][CH3:25])=[O:22])=[O:18])([CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[NH2:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 131726535HCID 131726535, 화합물

생성물 1

HCID 131726536HCID 131726536, 화합물

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 312751,4-Dioxane용매

실험 절차

[N-(tert-butyloxycarbonyl)-α-methyl-(R)-phenylalanyl]glycine, ethyl ester was stirred at ambient temperature in 4N HCl in dioxane (30 ml). After 1.5 h, the solvent was removed in vacuo. The residue was transferred to a separatory funnel with EtOAc. Extraction with EtOAc (2×) and washing of the combined organic layers brine and drying with MgSO4 afforded 0.63 g of crude product after evaporation of the solvent. This was used in the next step without further purification. MS (ESI) 265 (M+H).

후처리

  1. customthe solvent was removed in vacuo
  2. customThe residue was transferred to a separatory funnel with EtOAc
  3. extractionExtraction with EtOAc (2×)
  4. washwashing of the combined organic layers brine
  5. dry with materialdrying with MgSO4

출처 및 근거

ORD 기록
ord-dd1e7f4c3d7d40e98ca5b1523f44c9e8
출처 데이터셋
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07812024B2

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