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7,7-Dimethoxyheptanal → HCID 68902939、化合物

HRID 2101435
ノート
印刷プレビュー

反応式

HRID 2101435 の反応式
C(O)(=O)C1C=CC=CC=1.[CH:10]([NH:13][CH:14]1[CH2:19][CH2:18][N:17]([CH2:20][C:21]2[CH:22]=[N:23][CH:24]=[CH:25][C:26]=2[O:27][CH3:28])[CH2:16][CH2:15]1)([CH3:12])[CH3:11].[CH3:29][O:30][CH:31]([O:39][CH3:40])[CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH:37]=O.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClCCl>[CH3:40][O:39][CH:31]([O:30][CH3:29])[CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][N:13]([CH:10]([CH3:12])[CH3:11])[CH:14]1[CH2:15][CH2:16][N:17]([CH2:20][C:21]2[CH:22]=[N:23][CH:24]=[CH:25][C:26]=2[O:27][CH3:28])[CH2:18][CH2:19]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 5542747,7-Dimethoxyheptanal2 回HCID 5049666Sodium triacetoxyborohydride2 回HCID 674274674-Isopropylamino-1-(4-methoxypyrid-3-ylmethyl)piperidine monobenzoic acid salt

生成物 1

HCID 68902939HCID 68902939、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a reactor containing dichloromethane (4 L) was added 4-isopropylamino-1-(4-methoxypyrid-3-ylmethyl)piperidine monobenzoic acid salt (1.5 kg, 3.89 mol) while maintaining the temperature of the mixture at −5° C. to 5° C. The container used to add the salt was rinsed with dichloromethane (1.5 L) and the rinse was added to the reaction mixture. The temperature of the reaction mixture was then adjusted to 0° C. to 5° C. and 7,7-dimethoxyheptanal (790 g, 4.25 mol, 93.8% purity by GC) was added while maintaining the temperature of the reaction mixture between 0° C. to 5° C. The container used to add the 7,7-dimethoxyheptanal was rinsed with dichloromethane (0.8 L) and the rinse was added to the reactor. The resulting reaction mixture was then stirred at 0° C. to 5° C. for 1 hour. Sodium triacetoxyborohydride (1.07 kg, 5.05 mol) was then added in 7 equal portions over a period of 1 hour while maintaining the temperature of the reaction mixture between −5° C. to 5° C. The container used to add the sodium triacetoxyborohydride was rinsed with dichloromethane (0.8 L) and the rinse was added to the reaction mixture. The reaction mixture was then stirred at 0° C. to 5° C. for 21 hours. An aqueous solution of potassium carbonate (500 g) in deionized water (8.6 L) was then added to the reaction mixture while maintaining the temperature of the mixture between to 0° C. to 25° C. The resulting mixture was stirred for 2 hours at a temperature between 15° C. to 25° C. The layers were then allowed to separate over a period of 30 minutes and the organic layer was collected. The washing procedure with aqueous potassium carbonate solution was repeated 2 times. To the organic layer was then added an aqueous solution of sodium chloride (5.7 kg) in deionized water (15 L) while maintaining the temperature between to 15° C. to 25° C. The resulting mixture was stirred for 30 minutes at a temperature between 15° C. to 25° C. and then the layers were allowed to separate over a period of 30 minutes. The organic layer was collected and to this layer was added dichloromethane (1.5 L). The resulting solution containing the title compound was stored under a nitrogen atmosphere, protected from light, at 0° C. to 5° C. until used in the subsequent reaction.

後処理

  1. temperaturewhile maintaining the temperature of the mixture at −5° C. to 5° C
  2. additionto add the salt
  3. washwas rinsed with dichloromethane (1.5 L)
  4. additionthe rinse was added to the reaction mixture
  5. customwas then adjusted to 0° C. to 5° C.
  6. temperaturewhile maintaining the temperature of the reaction mixture between 0° C. to 5° C
  7. washwas rinsed with dichloromethane (0.8 L)
  8. additionthe rinse was added to the reactor
  9. customThe resulting reaction mixture
  10. temperaturewhile maintaining the temperature of the reaction mixture between −5° C. to 5° C
  11. washwas rinsed with dichloromethane (0.8 L)
  12. additionthe rinse was added to the reaction mixture
  13. stirringThe reaction mixture was then stirred at 0° C. to 5° C. for 21 hours
  14. additionAn aqueous solution of potassium carbonate (500 g) in deionized water (8.6 L) was then added to the reaction mixture
  15. temperaturewhile maintaining the temperature of the mixture between to 0° C. to 25° C
  16. stirringThe resulting mixture was stirred for 2 hours at a temperature between 15° C. to 25° C
  17. customto separate over a period of 30 minutes
  18. customthe organic layer was collected
  19. additionTo the organic layer was then added an aqueous solution of sodium chloride (5.7 kg) in deionized water (15 L)
  20. temperaturewhile maintaining the temperature between to 15° C. to 25° C
  21. stirringThe resulting mixture was stirred for 30 minutes at a temperature between 15° C. to 25° C.
  22. customto separate over a period of 30 minutes
  23. customThe organic layer was collected and to this layer
  24. additionwas added dichloromethane (1.5 L)
  25. additionThe resulting solution containing the title compound
  26. customprotected from light, at 0° C. to 5° C.
  27. customuntil used in the subsequent reaction

出典と根拠

ORDレコード
ord-7e11fd55f5c04b1484e20956394707b5
出典データセット
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07572918B2

反応ノート

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