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Triethylamine → HCID 86747110, 화합물

HRID 2081256
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HRID 2081256 반응식
[C:1]([O:5][C:6]([NH:8][CH2:9][C:10]([OH:12])=O)=[O:7])([CH3:4])([CH3:3])[CH3:2].C(N(CC)CC)C.ClC(OCC(C)C)=O.[CH2:28]([CH:35]([C:41]([OH:43])=[O:42])[C@@H:36]([C:38]([OH:40])=[O:39])[NH2:37])[C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1>C1COCC1.O>[C:1]([O:5][C:6]([NH:8][CH2:9][C:10]([NH:37][C@H:36]([C:38]([OH:40])=[O:39])[CH:35]([CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[C:41]([OH:43])=[O:42])=[O:12])=[O:7])([CH3:2])([CH3:3])[CH3:4]
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참가 물질

7

반응물 4

HCID 8471Triethylamine2회HCID 62365Isobutyl chloroformateHCID 78288N-(tert-butoxycarbonyl)glycineHCID 11665740beta-benzyl-L-aspartic acid

생성물 1

HCID 86747110HCID 86747110, 화합물수율 60.5%

시약·촉매·용매 2

HCID 962Water
용매
HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

5.3 g (30 mmol) of t-butoxycarbonyl glycine was dissolved in 100 ml of purified THF and 4.6 ml (33 mmol) of triethylamine and 4.33 ml (33 mmol) of isobutyl chloroformate) were added thereto at -15° C. The mixture was stirred at this temperature for 10 minutes. To the resultant solution of a mixed acid anhydride was added a solution which had been prepared by dissolving 8.0 g (36 mmol) of β-benzyl-L-aspartic acid and 5.02 ml (36 mmol) of triethylamine in water and cooling to 0° C. The mixture was then stirred at 0° C. for 1 hour and further at room temperature for 15 hours. After removing the THF by concentration under reduced pressure, cold 10% citric acid was added thereto. The precipitate thus formed was extracted with ethyl acetate twice. The extracts were combined and washed 5 times with one fifth the volume of 5% citric acid and then 10 times with water (one tenth the volume thereof). The solution was dehydrated over anhydrous sodium sulfate and concentrated to dryness. Then the residue was dissolved in ether and precipitated with n-hexane. After repeating this precipitation procedure 3 times, the obtained product was dried, whereby 6.9 g of the titled compound was obtained.

후처리

  1. customat -15° C
  2. customhad been prepared
  3. stirringThe mixture was then stirred at 0° C. for 1 hour and further at room temperature for 15 hours
  4. customAfter removing the THF
  5. concentrationby concentration under reduced pressure, cold 10% citric acid
  6. additionwas added
  7. customThe precipitate thus formed
  8. extractionwas extracted with ethyl acetate twice
  9. washwashed 5 times with one fifth the volume of 5% citric acid
  10. concentrationconcentrated to dryness
  11. dissolutionThen the residue was dissolved in ether
  12. customprecipitated with n-hexane
  13. customthis precipitation procedure 3 times
  14. customthe obtained product was dried

출처 및 근거

ORD 기록
ord-2211eef218774422b6de97c27a5579d7
출처 데이터셋
uspto-grants-1993_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05183804

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