Triethylamine → (R)-7-[3-(1-Amino-1-methylethyl)-1-pyrrolidinyl)-1-(2,4-difluorophenyl)-6-fluoro-1,4-dihydro-5-methyl-4-oxo-3-quinolinecarboxylic Acid
반응식
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[N:9]1[C:18]2[C:13](=[C:14]([CH3:21])[C:15]([F:20])=[C:16](F)[CH:17]=2)[C:12](=[O:22])[C:11]([C:23]([OH:25])=[O:24])=[CH:10]1.C([N:28]([CH2:31][CH3:32])[CH2:29][CH3:30])C>C(#N)C>[NH2:9][C:3]([C@@H:32]1[CH2:30][CH2:29][N:28]([C:16]2[CH:17]=[C:18]3[C:13]([C:12](=[O:22])[C:11]([C:23]([OH:25])=[O:24])=[CH:10][N:9]3[C:3]3[CH:4]=[CH:5][C:6]([F:8])=[CH:7][C:2]=3[F:1])=[C:14]([CH3:21])[C:15]=2[F:20])[CH2:31]1)([CH3:4])[CH3:2]참가 물질
실험 절차
A solution of 0.92 g (2.62 mmol) of 1-(2,4-difluorophenyl)-6,7-difluoro-1,4-dihydro-5-methyl-4-oxo-3-quinolinecarboxylic acid, 0.90 g (3.9 mmol) of (3R)-(1,-methyl-1'-t-butoxycarbonylaminoethyl)pyrrolidine (9a), 0.80 g (7.9 mmol) of triethylamine, and 50 mL of acetonitrile was heated at reflux for 18 hours. The solution was cooled to room temperature and concentrated in vacuo to an orange solid. The residue was chromatographed on E. Merck silica gel (230-400 mesh), eluting with 90:10 CHCl3:MeOH to give 1.47 g of (R) 7-[3-(1-t-butoxycarbonylamino-1-methylethyl)-1-pyrrolidinyl]-1-(2,4-difluorophenyl)-6-fluoro-1,4-dihydro-5-methyl-4-oxo-3-quinolinecarboxylic acid; NMR (CDCl3) δ8.47 (s, 1 H), 7.44 (m, 1 H), 7.15 (m, 2 H), 5.64 (d, J=7 HZ, 1 H), 4.47 (bs, 1 H), 3.50- 3.20 (m, 4 H), 2.85 (d, J=3.5 HZ, 3 H), 1.91 (m, 1 H), 1.74 (m, 2 H), 1.42 (s, 9 H), 1.29 (d, J=11 HZ, 6 H).
후처리
- temperatureat reflux for 18 hours
- concentrationconcentrated in vacuo to an orange solid
- customThe residue was chromatographed on E
- washMerck silica gel (230-400 mesh), eluting with 90:10 CHCl3
출처 및 근거
- ORD 기록
- ord-b79bb664d99f4e40a4f2e6f1d9846586
- 출처 데이터셋
- uspto-grants-1994_01
- 특허 번호
- US05278317
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