Ethanol → (3S,4R,6R)-3-ethenyl-6-[(S)-hydroxy-(6-methoxyquinolin-4-yl)methyl]-1-azabicyclo[2.2.2]octan-3-ol

HRID 982304ノート

反応式

HRID 982304 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[N:12]=[CH:11][CH:10]=[C:9]([C@H:13]([OH:24])[C@@H:14]3[N:19]4[CH2:20][C@H:21]([CH:22]=[CH2:23])[CH:16]([CH2:17][CH2:18]4)[CH2:15]3)[C:7]=2[CH:8]=1.C([OH:27])C>>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[C:7](=[C:9]([C@H:13]([OH:24])[C@@H:14]3[N:19]4[CH2:20][C@:21]([OH:27])([CH:22]=[CH2:23])[C@H:16]([CH2:17][CH2:18]4)[CH2:15]3)[CH:10]=[CH:11][N:12]=2)[CH:8]=1

参加物

3

反応物 2

HCID 702EthanolHCID 5953(S)-[(2R,5R)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxyquinolin-4-yl)methanol

生成物 1

HCID 124012(3S,4R,6R)-3-ethenyl-6-[(S)-hydroxy-(6-methoxyquinolin-4-yl)methyl]-1-azabicyclo[2.2.2]octan-3-ol

実験手順

A few drops of a suspension of M. plumbeus MMP 430 spores are added to 100 ml of medium A, described below, adjusted to pH7, in a 250 ml Erlenmeyer flask. Incubation is continued for 72 hours at 27° C. in a rotating agitator (327 RPM). A solution of 50 mg of quinidine in 1 ml of ethanol is then added under sterile conditions to the culture, and agitation is continued for 14 days under the same conditions. The culture is filtered on celite, the filtrate saturated with NaCl, brought to pH 10-12 by 2N NaOH, the extracted 6 times by methylene chloride. The dried and subsequently evaporated organic fractions are chromatographed on a preparative layer of silica gel, using as solvent CHCl2 -MeOH-NH4OH (85:14:1). The (3S)-3-hydroxy-quinidine band, identified by its fluorescence at 254 nm and its migration, which is smaller than that of quinidine, is scraped off and eluted by methanol. One obtains 1 mg of (3S)-3-hydroxy quinidine, identical with an authentic sample. Non-reacted quinidine is recovered in the same manner, and almost quantitatively (42 mg).

後処理

  1. additionplumbeus MMP 430 spores are added to 100 ml of medium A,
  2. waitis continued for 14 days under the same conditions
  3. filtrationThe culture is filtered on celite
  4. extractionthe extracted 6 times by methylene chloride
  5. customThe dried
  6. customsubsequently evaporated organic fractions are chromatographed on a preparative layer of silica gel
  7. washeluted by methanol

出典と根拠

ORDレコード
ord-2f8d9520113c43c3a57697cc9e50bd85
出典データセット
uspto-grants-1991_02
特許番号
US04996149

反応ノート

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