Methanol → HCID 14989222、化合物

HRID 484502ノート

反応式

HRID 484502 の反応式
[Na].Cl[C:3]1[N:8]=[N:7][C:6]([N:9]2[CH2:14][CH2:13][CH:12]([CH2:15][CH2:16][OH:17])[CH2:11][CH2:10]2)=[CH:5][CH:4]=1.[CH3:18][OH:19]>>[CH3:18][O:19][C:3]1[N:8]=[N:7][C:6]([N:9]2[CH2:14][CH2:13][CH:12]([CH2:15][CH2:16][OH:17])[CH2:11][CH2:10]2)=[CH:5][CH:4]=1

参加物

4

反応物 3

HCID 887MethanolHCID 5360545SodiumHCID 149892211-(6-Chloro-3-pyridazinyl)-4-piperidineethanol

生成物 1

HCID 14989222HCID 14989222、化合物収率 61.5%

実験手順

5.7 Parts of sodium (in pieces) were added to 86 parts of methanol. After the dropwise addition of 12.1 parts of 1-(6-chloro-3-pyridazinyl)-4-piperidineethanol, the reaction mixture was stirred overnight at reflux temperature. After cooling, the whole was poured into ice water and the product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of methylbenzene and methanol (90:10 by volume) as eluent. The desired fraction was collected and the eluent was evaporated, yielding 7.3 parts (61.5%) of 1-(6-methoxy-3-pyridazinyl)-4-piperidineethanol as a residue (int. 95).

後処理

  1. temperatureat reflux temperature
  2. temperatureAfter cooling
  3. extractionthe product was extracted with dichloromethane
  4. customThe extract was dried
  5. filtrationfiltered
  6. customevaporated
  7. customThe residue was purified by column chromatography over silica gel using
  8. additiona mixture of methylbenzene and methanol (90:10 by volume) as eluent
  9. customThe desired fraction was collected
  10. customthe eluent was evaporated

出典と根拠

ORDレコード
ord-2c8825e9c77a4fc08e2864ebf31b7761
出典データセット
uspto-grants-1993_07
特許番号
US05231184

反応ノート

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