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Triethylamine → (5R)-3-(6-chloro-3-pyridinyl)-5-ethyl-5-methyl-2,4-imidazolidinedione

HRID 527653
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HRID 527653 반응식
[Cl:1][C:2]1[N:7]=[CH:6][C:5]([NH2:8])=[CH:4][CH:3]=1.Cl.[NH2:10][C@:11]([CH3:17])([CH2:15][CH3:16])[C:12](O)=[O:13].C(P1(=O)OP(CCC)(=O)OP(CCC)(=O)O1)CC.CCN(CC)CC.Cl[C:44](Cl)([O:46]C(=O)OC(Cl)(Cl)Cl)Cl>CC#N.C(OCC)(=O)C.C(OCC)(=O)C>[Cl:1][C:2]1[N:7]=[CH:6][C:5]([N:8]2[C:12](=[O:13])[C@:11]([CH2:15][CH3:16])([CH3:17])[NH:10][C:44]2=[O:46])=[CH:4][CH:3]=1
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참가 물질

8

반응물 5

HCID 8471TriethylamineHCID 793055-Amino-2-chloropyridineHCID 94429TriphosgeneHCID 111923Propylphosphonic anhydrideHCID 17998883(R)-2-Amino-2-methylbutanoic acid hydrochloride

생성물 1

HCID 86698458(5R)-3-(6-chloro-3-pyridinyl)-5-ethyl-5-methyl-2,4-imidazolidinedione수율 198.2%

시약·촉매·용매 2

HCID 8857Ethyl Acetate용매2회HCID 21930812Acetonitrile ethyl acetate용매

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온도
60 °C

실험 절차

6-Chloropyridin-3-amine (3.0 g, 23.3 mmol) was dissolved in a 3:1 v/v mixture of CH3CN/ethyl acetate (20 mL) and (2R)-2-amino-2-methylbutanoic acid hydrochloride (3.97 g, 25.63 mmol) was added, followed by a 50% w/w solution in ethyl acetate of T3P (15.3 mL, 25.63). The mixture was heated to 60° C. for 2 hrs, then quenched with NaOH 3N while the pH was ˜10 and then diluted with ethyl acetate (100 mL). The organic phase was collected, dried over Na2SO4 and concentrated under vacuum to a final volume of ˜15 mL. The solution was cooled down to 0-5° C. and Et3N (11.4 ml, 81.9 mmol) was added. A solution of triphosgene (2.76 g, 6.96 mmol) in 10 mL of ethyl acetate was added drop wise in 15 min, keeping the internal temperature below 5° C. The mixture was stirred at 5° C. for 30 minutes then quenched with water (100 mL) and finally diluted with additional ethyl acetate (100 mL). Two phases were separated and the organic layer was washed with water and brine, dried over Na2SO4 and concentrated under vacuum. The crude product was suspended in 15 mL of ethyl acetate followed by the drop wise addition of 65 mL of n-heptane. The resulting suspension was stirred at room temperature for 2 hrs, filtered, and the cake washed with a 2:8 v/v mixture of ethyl acetate/n-heptane (2×10 mL) before being dried at 40° C. for 18 hrs affording the title compound (3.5 g) as white solid.

후처리

  1. additionwas added
  2. customquenched with NaOH 3N while the pH was ˜10
  3. additiondiluted with ethyl acetate (100 mL)
  4. customThe organic phase was collected
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated under vacuum to a final volume of ˜15 mL
  7. temperatureThe solution was cooled down to 0-5° C.
  8. customthe internal temperature below 5° C
  9. customthen quenched with water (100 mL)
  10. additionfinally diluted with additional ethyl acetate (100 mL)
  11. customTwo phases were separated
  12. washthe organic layer was washed with water and brine
  13. dry with materialdried over Na2SO4
  14. concentrationconcentrated under vacuum
  15. additionfollowed by the drop wise addition of 65 mL of n-heptane
  16. stirringThe resulting suspension was stirred at room temperature for 2 hrs
  17. filtrationfiltered
  18. washthe cake washed with a 2:8 v/v mixture of ethyl acetate/n-heptane (2×10 mL)
  19. custombefore being dried at 40° C. for 18 hrs

출처 및 근거

ORD 기록
ord-cdb9620f18354544b92b28dd96d484b0
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09346790B2

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