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Hydrochloric Acid → ethyl 2-(1-(1,3-diethoxy-2-propoxycarbonyloxy)-2-methylpropyl)-5-(5-isopropoxy-4-methoxy-2-nitrobenzoyl)-2H-1,2,3-triazole-4-carboxylate

HRID 1293571
ノート
印刷プレビュー

反応式

HRID 1293571 の反応式
O.[C:2]1([CH3:12])[CH:7]=CC(S(O)(=O)=O)=C[CH:3]=1.[CH:13]([O:16][C:17]1[C:18]([O:38][CH3:39])=[CH:19][C:20]([N+:35]([O-:37])=[O:36])=[C:21]([CH:34]=1)[C:22]([C:24]1[NH:28][N:27]=[N:26][C:25]=1[C:29]([O:31][CH2:32][CH3:33])=[O:30])=[O:23])([CH3:15])[CH3:14].C(N1C=CN=C1)(N1C=CN=C1)=O.[CH2:52]([O:54][CH2:55][CH:56]([OH:61])[CH2:57][O:58][CH2:59][CH3:60])[CH3:53].FC(F)(F)[C:64]([OH:66])=[O:65].Cl>C(Cl)Cl>[CH2:52]([O:54][CH2:55][CH:56]([O:61][C:64]([O:66][CH:7]([N:27]1[N:26]=[C:25]([C:29]([O:31][CH2:32][CH3:33])=[O:30])[C:24]([C:22](=[O:23])[C:21]2[CH:34]=[C:17]([O:16][CH:13]([CH3:15])[CH3:14])[C:18]([O:38][CH3:39])=[CH:19][C:20]=2[N+:35]([O-:37])=[O:36])=[N:28]1)[CH:2]([CH3:3])[CH3:12])=[O:65])[CH2:57][O:58][CH2:59][CH3:60])[CH3:53]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 6

HCID 313Hydrochloric AcidHCID 6422Trifluoroacetic acidHCID 682631,1'-CarbonyldiimidazoleHCID 776641,3-Diethoxy-2-propanolHCID 521998p-Toluenesulfonic acid monohydrateHCID 178470513HCID 178470513、化合物

生成物 1

HCID 69470612
ethyl 2-(1-(1,3-diethoxy-2-propoxycarbonyloxy)-2-methylpropyl)-5-(5-isopropoxy-4-methoxy-2-nitrobenzoyl)-2H-1,2,3-triazole-4-carboxylate

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
-30 °C

実験手順

p-Toluenesulfonic acid monohydrate (57 mg) and isobutyl aldehyde (0.41 ml) were added to a solution of ethyl 5-(5-isopropoxy-4-methoxy-2-nitrobenzoyl)-1H-1,2,3-triazole-4-carboxylate (1.14 g), prepared in step (32a), in methylene chloride solution (17 ml) at −20° C. The mixture was stirred at that temperature for one hr. 1,1′-Carbonyldiimidazole (732 mg) was added to the reaction solution. Further; one hr after that, 1,3-diethoxy-2-propanol (4.70 ml) was added thereto. The reaction solution was cooled to −30° C. Trifluoroacetic acid (0.70 ml) was added thereto. The temperature was raised to room temperature, followed by stirring for 25 hr. 0.5 M hydrochloric acid was added to the reaction solution under ice cooling to stop the reaction, and separation was then carried out. The organic layer was washed five times with a 7% aqueous sodium hydrogencarbonate solution. The solvent was evaporated under reduced pressure. Diethyl ether and water were added to the residue. The organic layer after the separation was successively washed twice with water, with 0.5 M hydrochloric acid, twice with water, and then with 20% saline. The solvent was evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (ethyl acetate/hexane) to give a crude product of ethyl 2-(1-(1,3-diethoxy-2-propoxycarbonyloxy)-2-methylpropyl)-5-(5-isopropoxy-4-methoxy-2-nitrobenzoyl)-2H-1,2,3-triazole-4-carboxylate (1.15 g).

後処理

  1. temperatureThe temperature was raised to room temperature
  2. stirringby stirring for 25 hr
  3. customthe reaction, and separation
  4. washThe organic layer was washed five times with a 7% aqueous sodium hydrogencarbonate solution
  5. customThe solvent was evaporated under reduced pressure
  6. additionDiethyl ether and water were added to the residue
  7. customThe organic layer after the separation
  8. washwas successively washed twice with water, with 0.5 M hydrochloric acid, twice with water
  9. customThe solvent was evaporated under reduced pressure
  10. customThe residue was purified by column chromatography on silica gel (ethyl acetate/hexane)

出典と根拠

ORDレコード
ord-bd4b401b2f3449f99f6ebe7d87cb1cfa
出典データセット
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07238812B2

反応ノート

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