Sodium Carbonate → HCID 20371485、化合物

HRID 616220

反応式

HRID 616220 の反応式
C(=O)([O-])[O-].[Na+].[Na+].[CH:7]1[C:17]2[CH2:16][CH2:15][C:14]3[CH:18]=[CH:19][CH:20]=[CH:21][C:13]=3[C:12](=[C:22]3[CH2:27][CH2:26][NH:25][CH2:24][CH2:23]3)[C:11]=2[CH:10]=[CH:9][CH:8]=1.Br[CH2:29][CH2:30][CH2:31][C:32](=[O:34])[CH3:33]>C(Cl)(Cl)Cl>[CH:7]1[C:17]2[CH2:16][CH2:15][C:14]3[CH:18]=[CH:19][CH:20]=[CH:21][C:13]=3[C:12](=[C:22]3[CH2:23][CH2:24][N:25]([CH2:29][CH2:30][CH2:31][C:32](=[O:34])[CH3:33])[CH2:26][CH2:27]3)[C:11]=2[CH:10]=[CH:9][CH:8]=1

参加物

5

反応物 3

HCID 10340Sodium CarbonateHCID 774932-Pentanone, 5-bromo-HCID 1201458Desloratadine impurity 24

生成物 1

HCID 20371485HCID 20371485、化合物

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒2 回

実験手順

9.2 g of sodium carbonate are added to a solution of 10 g of 4-(10,11-dihydro-5-dibenzo[a,d]cycloheptenylidene)piperidine in 100 cc of chloroform, a solution of 7.2 g of 5-bromo-2-pentanone in 50 cc of chloroform is then added dropwise within 20 minutes, and the mixture is subsequently boiled at reflux for 17 hours. After cooling, the precipitate is filtered off, the filtrate is extracted twice with water, dried over magnesium sulphate and concentrated by evaporation. The residue is filtered over a column of 170 g of silica gel. The fraction eluted with chloroform containing 1% of methanol is dissolved in acetone and acidifed with hydrogen chloride in ether. After the addition of more ether, the hydrochloride of the title compound crystallizes. M.P. 235°-238°.

後処理

  1. temperatureat reflux for 17 hours
  2. temperatureAfter cooling
  3. filtrationthe precipitate is filtered off
  4. extractionthe filtrate is extracted twice with water
  5. dry with materialdried over magnesium sulphate
  6. concentrationconcentrated by evaporation
  7. filtrationThe residue is filtered over a column of 170 g of silica gel
  8. washThe fraction eluted with chloroform containing 1% of methanol
  9. dissolutionis dissolved in acetone
  10. additionAfter the addition of more ether
  11. customthe hydrochloride of the title compound crystallizes

出典と根拠

ORDレコード
ord-3373ca92e5484e05bbc60f90bbe439f1
出典データセット
uspto-grants-1978_02
特許番号
US04072756

関連ノート

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