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1-Hydroxybenzotriazole → 2-(2-Morpholin-4-yl-2-oxo-ethyl)-2-(3-phenyl-propyl)-malonic acid monoethyl ester

HRID 1830202
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HRID 1830202 반응식
[CH:1]1(N=C=N)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.N1(C(=O)CC(=C)[C:19]([OH:21])=[O:20])CCOCC1.C1C=CC2N([OH:33])N=NC=2C=1.O1C2C=CC=CC=2N=C1[C:43]([C@@H:45]([NH:49][C:50](=O)[CH:51](CS(CC1C=CC=CC=1C(F)(F)F)(=O)=O)CS(CC1C=CC=CC=1C(F)(F)F)(=O)=O)CCC)=[O:44].CCN([CH:89]([CH3:91])C)C(C)C.CC(OI1(OC(C)=O)(OC(C)=O)[O:105][C:103](=[O:104])[C:102]2[CH:101]=[CH:100][CH:99]=[CH:98][C:97]1=2)=O>C(Cl)Cl>[CH2:89]([O:21][C:19](=[O:20])[C:102]([CH2:97][C:98]([N:49]1[CH2:45][CH2:43][O:44][CH2:51][CH2:50]1)=[O:33])([CH2:101][CH2:100][CH2:99][C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1)[C:103]([OH:105])=[O:104])[CH3:91]
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참가 물질

8

반응물 6

HCID 757711-HydroxybenzotriazoleHCID 81531DiisopropylethylamineHCID 159087TriacetoxyperiodinaneHCID 10212428N-[(S)-1-(1-Benzooxazol-2-yl-methanoyl)-butyl]-3-(2-trifluoromethyl-benzylsulfonyl)-2-(2-trifluoromethyl-benzylsulfonylmethyl)-propionamideHCID 12048208N-CyclohexylcarbodiimideHCID 22054022
2-Methylene4-morpholin-4-yl-4-oxo-butyric acid

생성물 1

HCID 210256902-(2-Morpholin-4-yl-2-oxo-ethyl)-2-(3-phenyl-propyl)-malonic acid monoethyl ester

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a stirring suspension of N-Cyclohexylcarbodiimide, N′-methyl polystyrene resin (1.7 mmole/gram, 0.3529 g, 0.6 mmol) in 10 ml of methylene chloride was added the acid 1 (98.2 mg, 0.3 mmol) and HOBT (69 mg, 0.51 mmol) which was allowed to stir for 15 minutes at room temperature. Compound 2 (80.6 mg, 0.3 mmol) and DIEA (0.1 ml, 0.5 mmol) were added and the reaction was allowed to stir for 5 hours at room temperature. Then silicycle triamine™ (0.42 g, 1.5 mmol) was added and the reaction was stirred overnight at room temperature. The reaction was filtered and the solvent was removed under reduced pressure. The crude product 3 was used without further purification. Crude compound 3 was dissolved in methylene chloride and Dess-Martin reagent (15% in methylene chloride, 1.13 g, 0.6 mmol) was added and the reaction was allowed to stir at room temperature for 3 hours. The excess Dess-Martin reagent was consumed by adding sodium thiosulfate in saturated sodium bicarbonate. The product was extracted with ethyl acetate and washed with brine. The organic layer was dried over magnesium sulfate, filtered and concentrated under reduced pressure. The product was purified using HPLC to yield 15 mg of final compound 4; LCMS retention time 3:07 minutes, M+1(540.2).

후처리

  1. stirringto stir for 5 hours at room temperature
  2. stirringthe reaction was stirred overnight at room temperature
  3. filtrationThe reaction was filtered
  4. customthe solvent was removed under reduced pressure
  5. customThe crude product 3 was used without further purification
  6. dissolutionCrude compound 3 was dissolved in methylene chloride
  7. stirringto stir at room temperature for 3 hours
  8. customThe excess Dess-Martin reagent was consumed
  9. additionby adding sodium thiosulfate in saturated sodium bicarbonate
  10. extractionThe product was extracted with ethyl acetate
  11. washwashed with brine
  12. dry with materialThe organic layer was dried over magnesium sulfate
  13. filtrationfiltered
  14. concentrationconcentrated under reduced pressure
  15. customThe product was purified

출처 및 근거

ORD 기록
ord-6df837c0dafc4ef3812e0cec87e8303e
출처 데이터셋
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07064123B1

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