(S)-tert-Butyl 5-azaspiro[2.4]heptan-7-ylcarbamate → 7-[7-(S)-Amino-5-azaspiro[2.4]heptan-5-yl]-6-fluoro-1-[(1R,2S)-2-fluorocyclopropyl]-5-methyl-4-oxo-1,4-dihydroquinoline-3-carboxylic Acid
반응식
[F:1][C:2]1[C:3]([CH3:21])=[C:4]2[C:9](=[CH:10][C:11]=1F)[N:8]([C@@H:13]1[CH2:15][C@@H:14]1[F:16])[CH:7]=[C:6]([C:17]([OH:19])=[O:18])[C:5]2=[O:20].C(OC([NH:29][C@H:30]1[C:34]2([CH2:36][CH2:35]2)[CH2:33][NH:32][CH2:31]1)=O)(C)(C)C>CS(C)=O>[NH2:29][C@H:30]1[C:34]2([CH2:36][CH2:35]2)[CH2:33][N:32]([C:11]2[CH:10]=[C:9]3[C:4]([C:5](=[O:20])[C:6]([C:17]([OH:19])=[O:18])=[CH:7][N:8]3[C@@H:13]3[CH2:15][C@@H:14]3[F:16])=[C:3]([CH3:21])[C:2]=2[F:1])[CH2:31]1참가 물질
반응물 2
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- 100 °C
실험 절차
A mixture of 200 mg of 6,7-difluoro-1-[(1R,2S)-2-fluorocyclopropyl]-5-methyl-4-oxo-1,4-dihydroquinoline-3-carboxylic acid, 287 mg of 7-(S)-t-butoxycarbonylamino-5-azaspiro[2.4]heptane, and 5 ml of anhydrous dimethyl sulfoxide was heated at 100° C. for 30 minutes with stirring. After allowing to cool, the reaction mixture was concentrated under reduced pressure, and water was added to the residue. The precipitated yellow crystals were collected by filtration and added to 5 ml of trifluoroacetic acid while stirring and cooling with ice, followed by stirring at room temperature for 30 minutes. The reaction mixture was further worked up in the same manner as in Example 7. Recrystallization of the crude crystal from ethanol gave 122 mg of the titled compound as a pale yellow powder.
후처리
- temperatureto cool
- concentrationthe reaction mixture was concentrated under reduced pressure, and water
- additionwas added to the residue
- filtrationThe precipitated yellow crystals were collected by filtration
- additionadded to 5 ml of trifluoroacetic acid
- stirringwhile stirring
- temperaturecooling with ice
- stirringby stirring at room temperature for 30 minutes
- customRecrystallization of the crude crystal from ethanol
출처 및 근거
- ORD 기록
- ord-ade5edcba9304a37ad800bcd93be1e42
- 출처 데이터셋
- uspto-grants-1997_12
- 특허 번호
- US05696132
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