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Piperidine → Ethyl 2-acetoxymethyl-4-(3-chlorophenyl)-6-methyl-5-(3-phenyl-2-propene-1-ylcarbamoyl)-1,4-dihydropyridine-3-carboxylate

HRID 1700341
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HRID 1700341 반응식
O=[C:2]([CH3:16])[CH2:3][C:4]([NH:6][CH2:7][CH:8]=[CH:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[O:5].[Cl:17][C:18]1[CH:19]=[C:20]([CH:23]=[CH:24][CH:25]=1)[CH:21]=O.[NH:26]1CCCCC1.[C:32]([O:35][CH2:36][C:37](=O)[CH2:38][C:39]([O:41][CH2:42][CH3:43])=[O:40])(=[O:34])[CH3:33].C([O-])(=O)C.[NH4+]>C1C=CC=CC=1.CC(O)C.O>[C:32]([O:35][CH2:36][C:37]1[NH:26][C:2]([CH3:16])=[C:3]([C:4](=[O:5])[NH:6][CH2:7][CH:8]=[CH:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:21]([C:20]2[CH:23]=[CH:24][CH:25]=[C:18]([Cl:17])[CH:19]=2)[C:38]=1[C:39]([O:41][CH2:42][CH3:43])=[O:40])(=[O:34])[CH3:33]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

9

반응물 5

HCID 8082PiperidineHCID 114773-ChlorobenzaldehydeHCID 517165Ammonium AcetateHCID 11480907Ethyl 4-acetoxyacetoacetateHCID 53935748HCID 53935748, 화합물

생성물 1

HCID 70158280Ethyl 2-acetoxymethyl-4-(3-chlorophenyl)-6-methyl-5-(3-phenyl-2-propene-1-ylcarbamoyl)-1,4-dihydropyridine-3-carboxylate

시약·촉매·용매 3

HCID 241Benzene용매HCID 962Water용매HCID 3776Isopropanol용매2회

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온도
120 °C

실험 절차

652 mg (3.00 mmol) of 3-oxo-N-(3-phenyl-2-propene-1-yl)butyramide, 0.510 ml (3.00 mmol) of 3-chlorobenzaldehyde and 0.045 ml (0.30 mmol) of piperidine were heated under reflux in 37.5 ml of benzene overnight while water was removed. The reaction solution was washed with water and then dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The residue thus obtained, 564 mg (3.0 mmol) of ethyl 4-acetoxy-3-oxobutyrate and 278 mg (3.6 mmol) of ammonium acetate were heated at 80° C. under stirring in 15 ml of 2-propanol for four nights. The reaction mixture was then heated at 120° C. under stirring under atmospheric pressure for 4 hours while 2-propanol was evaporated. The residue was purified by the silica gel chromatography (hexane/ethyl acetate=1/2) to obtain the title compound.

후처리

  1. customwas removed
  2. washThe reaction solution was washed with water
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customThe solvent was evaporated under reduced pressure
  5. customThe residue thus obtained
  6. customwas evaporated
  7. customThe residue was purified by the silica gel chromatography (hexane/ethyl acetate=1/2)

출처 및 근거

ORD 기록
ord-41a7643709914e13bef254f4c94c4da6
출처 데이터셋
uspto-grants-2002_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06350762B1

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