1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → (R)-2-(4-Fluoro-3,5-dimethyl-phenylamino)-hexanoic acid tert-butoxy-amide
반응식
[F:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5]([NH:9][C@H:10]([CH2:14][CH2:15][CH2:16][CH3:17])[C:11]([OH:13])=O)=[CH:4][C:3]=1[CH3:18].[C:19]([O:23][NH2:24])([CH3:22])([CH3:21])[CH3:20].C1C=CC2N(O)N=NC=2C=1.C[N+]1(C)[C@H]2CC3C=CC(O)=C4O[C@H]5[C@@H](O)C=C[C@@H]2[C@]5(C=34)CC1.CCN=C=NCCCN(C)C>ClCCl.O>[C:19]([O:23][NH:24][C:11](=[O:13])[C@H:10]([NH:9][C:5]1[CH:4]=[C:3]([CH3:18])[C:2]([F:1])=[C:7]([CH3:8])[CH:6]=1)[CH2:14][CH2:15][CH2:16][CH3:17])([CH3:22])([CH3:21])[CH3:20]참가 물질
반응물 5
생성물 1
시약·촉매·용매 2
실험 절차
To a solution of crude (R)-2-(4-fluoro-3,5-dimethyl-phenylamino)-hexanoic acid (ca. 6.0 mmol), O-tert-butyl-hydroxyamine (2.261 g, 18.0 mmol), HOBT (0.811 g, 6.0 mmol), and N-methyl morphine (3.036 g, 30.0 mmol) in 20 mL of dichloromethane, was added EDCI (1.725 g, 9.0 mmol). After stirring at room temperature under N2 for 44 h, the reaction mixture was diluted with 60 mL of water and extracted with dichloromethane (60 mL×3). The organic extracts were combined and dried over anhydrous Na2SO4 and the solvents removed under reduced pressure. The product was isolated by Flash chromatography (silica gel) eluting with 0-30% ethyl acetate/hexanes to give the title compound as a pale yellow semi-solid (0.747 g, 38% yield). LC-MS: tR=8.8 min; m/z 325 (M+H)+.
후처리
- extractionextracted with dichloromethane (60 mL×3)
- dry with materialdried over anhydrous Na2SO4
- customthe solvents removed under reduced pressure
- customThe product was isolated by Flash chromatography (silica gel)
- washeluting with 0-30% ethyl acetate/hexanes
출처 및 근거
- ORD 기록
- ord-1ff177eb7e8149a3a056da007a31c06c
- 출처 데이터셋
- uspto-grants-2012_08
- 특허 번호
- US08242174B2
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