Diisopropylethylamine → (1-{1-[5-(4-Fluoro-phenyl)-2-methyl-thiazol-4-yl]-methanoyl}-piperidin-2-yl)-acetic acid methyl ester
반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[S:12][C:11]([CH3:13])=[N:10][C:9]=2[C:14]([OH:16])=O)=[CH:4][CH:3]=1.C(N(CC)C(C)C)(C)C.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[CH3:50][O:51][C:52](=[O:60])[CH2:53][CH:54]1[CH2:59][CH2:58][CH2:57][CH2:56][NH:55]1>CN(C=O)C.O>[CH3:50][O:51][C:52](=[O:60])[CH2:53][CH:54]1[CH2:59][CH2:58][CH2:57][CH2:56][N:55]1[C:14]([C:9]1[N:10]=[C:11]([CH3:13])[S:12][C:8]=1[C:5]1[CH:4]=[CH:3][C:2]([F:1])=[CH:7][CH:6]=1)=[O:16]참가 물질
7
반응물 4
생성물 1
시약·촉매·용매 2
실험 절차
A stirring solution of 5-(4-fluoro-phenyl)-2-methyl-thiazole-4-carboxylic acid (3.00 g, 12.5 mmol) in DMF (50 ml), under argon was treated sequentially with N,N-diisopropylethylamine (6.8 ml), HATU (4.77 g, 12.5 mmol) then after stirring for 0.25 h, piperidin-2-yl-acetic acid methyl ester (Beckett et al, J. Med. Chem., 563, 1969) (1.83 g, 12.5 mmol) was added. The mixture was stirred for 16 h at room temperature and was then diluted with water. The product was extracted into diethyl ether. The organic phase was washed with water (3×) and brine, was dried (MgSO4) and the solvent removed in vacuo to afford the title compound as a yellow gum (4.00 g, 85%).
후처리
- stirringThe mixture was stirred for 16 h at room temperature
- extractionThe product was extracted into diethyl ether
- washThe organic phase was washed with water (3×) and brine
- dry with materialwas dried (MgSO4)
- customthe solvent removed in vacuo
출처 및 근거
- ORD 기록
- ord-51704a145b694bb889574a8432feca5b
- 출처 데이터셋
- uspto-grants-2011_03
- 특허 번호
- US07897618B2
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