Ethylmorpholine → 3-Amino-N-(4-amino-2-methyl-quinolin-6-yl)-propionamide

HRID 19511

반응식

HRID 19511 반응식
C(OC(NCCC(O)=O)=O)(C)(C)C.[B-](F)(F)(F)F.CCO[C:22]([C:24]([C:34]#[N:35])=NOC(N(C)C)=[N+](C)C)=[O:23].[CH3:36][C:37]1[CH:46]=[C:45]([NH2:47])[C:44]2[C:39](=[CH:40][CH:41]=[C:42]([NH2:48])[CH:43]=2)[N:38]=1.C(N1CCOCC1)C>CN(C=O)C>[NH2:35][CH2:34][CH2:24][C:22]([NH:48][C:42]1[CH:43]=[C:44]2[C:39](=[CH:40][CH:41]=1)[N:38]=[C:37]([CH3:36])[CH:46]=[C:45]2[NH2:47])=[O:23]

참가 물질

6

실험 절차

To a solution of 2.18 g (11.55 mmol) of 3-tert-Butoxycarbonylamino-propionic acid in 20 ml of DMF were added 3.78 g (11.55 mmol) TOTU. After 15 min at room temperature 2.0 g (11.55 mmol) of 2-methyl-quinoline-4,6-diamine and 2.66 g (23 mmol) of N-ethylmorpholine were added. After 24 h stirring at room temperature the solution was evaporated and the residue was treated with a saturated aqueous solution of NaHCO3. The aqueous solution was extracted with ethyl acetate. The separated organic layer was dried (Na2SO4) and evaporated. The residue was treated with 20 ml 90% trifluoroacetic acid for 2 h. After evaporation the residue was dissolve in water and extracted with ethyl acetate. The aqueous layer was lyophilized to yield 5.15 g (76%) of the title compound. MS 245.1 (M+1)+.

후처리

  1. customwas evaporated
  2. additionthe residue was treated with a saturated aqueous solution of NaHCO3
  3. extractionThe aqueous solution was extracted with ethyl acetate
  4. dry with materialThe separated organic layer was dried (Na2SO4)
  5. customevaporated
  6. additionThe residue was treated with 20 ml 90% trifluoroacetic acid for 2 h
  7. customAfter evaporation the residue
  8. dissolutionwas dissolve in water
  9. extractionextracted with ethyl acetate

출처 및 근거

ORD 기록
ord-99c24b8d550d47829af6789f822fc3fc
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07745443B2

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