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Water → HCID 68511336、化合物

HRID 1717305
ノート
印刷プレビュー

反応式

HRID 1717305 の反応式
[CH:1]1([CH2:6][C:7](=O)[CH2:8][C:9]([O:11]CC)=[O:10])[CH2:5][CH2:4][CH2:3][CH2:2]1.[N:15]([C:18]1[CH:28]=[CH:27][C:21]([C:22]([NH:24][CH2:25][CH3:26])=[O:23])=[CH:20][CH:19]=1)=[N+:16]=[N-:17].[O-]CC.[Na+].O>C(O)C>[CH:1]1([CH2:6][C:7]2[N:15]([C:18]3[CH:19]=[CH:20][C:21]([C:22]([NH:24][CH2:25][CH3:26])=[O:23])=[CH:27][CH:28]=3)[N:16]=[N:17][C:8]=2[C:9]([OH:11])=[O:10])[CH2:2][CH2:3][CH2:4][CH2:5]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 2723922Sodium ethoxideHCID 23500382Ethyl 4-cyclopentyl-3-oxobutanoateHCID 594322264-azido-N-ethylbenzamide

生成物 1

HCID 68511336HCID 68511336、化合物収率 90.2%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒2 回

実験手順

Ethyl 4-cyclopentyl-3-oxobutyrate (0.781 g, 3.94 mmol, 1.25 eq.) obtained in Example 103a) and 4-azido-N-ethylbenzamide (0.60 g, 3.15 mmol) were dissolved in ethanol (20 ml), sodium ethoxide (298 mg, 3.94 mmol, 1.25 eq.) was added, and the mixture was stirred at room temperature for 30 min, and then at 50° C. for 12 hr. Water (20 ml) was added to the reaction mixture, ethanol was evaporated, and the residue was diluted with 2% aqueous sodium carbonate solution (20 ml) and washed with ethyl acetate-hexane (2:1, 50 ml). The organic layer was extracted with 2% aqueous sodium carbonate solution (20 ml). The aqueous layers were combined, acidified (pH<3) with 6N hydrochloric acid, and extracted with ethyl acetate (35 ml and 30 ml). The organic layers were combined, washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated, and diethyl ether and ethyl acetate were added. The precipitate was collected by filtration, washed with diethyl ether and dried to give the title compound as a pale-yellow powder (971 mg, 2.84 mmol, 90.0%).

後処理

  1. waitat 50° C. for 12 hr
  2. customwas evaporated
  3. additionthe residue was diluted with 2% aqueous sodium carbonate solution (20 ml)
  4. washwashed with ethyl acetate-hexane (2:1, 50 ml)
  5. extractionThe organic layer was extracted with 2% aqueous sodium carbonate solution (20 ml)
  6. extractionextracted with ethyl acetate (35 ml and 30 ml)
  7. washwashed with saturated brine
  8. dry with materialdried over anhydrous sodium sulfate
  9. concentrationconcentrated
  10. additiondiethyl ether and ethyl acetate were added
  11. filtrationThe precipitate was collected by filtration
  12. washwashed with diethyl ether
  13. customdried

出典と根拠

ORDレコード
ord-e0073aaa435a4547a6b1f25f7c2448e9
出典データセット
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07803822B2

反応ノート

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