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
반응물 4
생성물 1
시약·촉매·용매 1
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
- customwas evaporated
- additionthe residue was treated with a saturated aqueous solution of NaHCO3
- extractionThe aqueous solution was extracted with ethyl acetate
- dry with materialThe separated organic layer was dried (Na2SO4)
- customevaporated
- additionThe residue was treated with 20 ml 90% trifluoroacetic acid for 2 h
- customAfter evaporation the residue
- dissolutionwas dissolve in water
- extractionextracted with ethyl acetate
출처 및 근거
- ORD 기록
- ord-99c24b8d550d47829af6789f822fc3fc
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07745443B2
연결된 노트
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