1,8-Diazabicyclo(5.4.0)undec-7-ene → 7-(cis-3-t-Butoxycarbonylamino-4-methyl-1-pyrrolidinyl)-6,8-difluoro-1-(2-fluoroethyl)-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid

HRID 580590노트

반응식

HRID 580590 반응식
[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[C:10]([F:13])[C:11]=1F)[N:8]([CH2:14][CH2:15][F:16])[CH:7]=[C:6]([C:17]([OH:19])=[O:18])[C:5]2=[O:20].[C:21]([O:25][C:26]([NH:28][C@H:29]1[C@@H:33]([CH3:34])[CH2:32][NH:31][CH2:30]1)=[O:27])([CH3:24])([CH3:23])[CH3:22].C1CCN2C(=NCCC2)CC1>C(#N)C>[C:21]([O:25][C:26]([NH:28][C@H:29]1[C@@H:33]([CH3:34])[CH2:32][N:31]([C:11]2[C:10]([F:13])=[C:9]3[C:4]([C:5](=[O:20])[C:6]([C:17]([OH:19])=[O:18])=[CH:7][N:8]3[CH2:14][CH2:15][F:16])=[CH:3][C:2]=2[F:1])[CH2:30]1)=[O:27])([CH3:24])([CH3:22])[CH3:23]

참가 물질

5

실험 절차

A mixture of 6,7,8-trifluoro-1-(2-fluoroethyl)-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid (0.5 g), anhydrous acetonitrile (5 ml), cis-3-t-butoxycarbonylamino-4-methylpyrrolidine (0.5 g) and DBU (0.27 g) was refluxed for an hour and then concentrated. The resulting residue was dissolved in chloroform and the solution was washed with 10% aqueous citric acid solution. After concentration of the chloroform layer, the resulting precipitate was triturated in water, and collected by filtration and washed with water, methanol and ether successively to give the title compound (0.51 g) as white powder, mp 217°-219° C.

후처리

  1. temperaturewas refluxed for an hour
  2. concentrationconcentrated
  3. dissolutionThe resulting residue was dissolved in chloroform
  4. washthe solution was washed with 10% aqueous citric acid solution
  5. customAfter concentration of the chloroform layer, the resulting precipitate was triturated in water
  6. filtrationcollected by filtration
  7. washwashed with water, methanol and ether successively

출처 및 근거

ORD 기록
ord-c6b8985c7fac49b795c3d29364acab73
출처 데이터셋
uspto-grants-1988_06
특허 번호
US04753953

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