HCID 10976898, 화합물 → HCID 20277264, 화합물

HRID 894725노트

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HRID 894725 반응식
[C:1]([C:3]1[CH:19]=[CH:18][CH:17]=[CH:16][C:4]=1[CH:5]=[C:6]([C:13]([CH3:15])=O)[C:7]([O:9]CCCl)=[O:8])#[N:2].[NH2:20]/[C:21](/[CH:28]([O:32][CH2:33][CH3:34])[O:29][CH2:30][CH3:31])=[CH:22]\[C:23]([O:25][CH2:26][CH3:27])=[O:24]>C(OCC)(=O)C>[C:1]([C:3]1[CH:19]=[CH:18][CH:17]=[CH:16][C:4]=1[CH:5]1[C:22]([C:23]([O:25][CH2:26][CH3:27])=[O:24])=[C:21]([CH:28]([O:32][CH2:33][CH3:34])[O:29][CH2:30][CH3:31])[NH:20][C:13]([CH3:15])=[C:6]1[C:7]([OH:9])=[O:8])#[N:2]

참가 물질

4

실험 절차

A mixture of 2-chloroethyl 2-(2-cyanobenzylidene)acetoacetate (4.72 g) and ethyl 3-amino-4,4-diethoxycrotonate (4.06 g) was heated for 3 hours at 100~105° C. with stirring. After cooling, the reaction mixture was dissolved in ethyl acetate, and the solution was washed twice with an aqueous solution of sodium chloride and then dried over magnesium sulfate. After removal of the solvent under reduced pressure, the residual oil was chromatographed over silica gel with a mixture of benzene and ethyl acetate (5:1 V/V) to give 2-chloroethyl ester of 4-(2-cyanophenyl)-5-ethoxycarbonyl-6-diethoxymethyl-2-methyl-1,4-dihydropyridine-3-carboxylic acid (5.81 g).

후처리

  1. temperaturewas heated for 3 hours at 100~105° C.
  2. temperatureAfter cooling
  3. washthe solution was washed twice with an aqueous solution of sodium chloride
  4. dry with materialdried over magnesium sulfate
  5. customAfter removal of the solvent under reduced pressure
  6. customthe residual oil was chromatographed over silica gel with a mixture of benzene and ethyl acetate (5:1 V/V)

출처 및 근거

ORD 기록
ord-98d06d6d4bc74f4ab531df5ee852eaa6
출처 데이터셋
uspto-grants-1981_08
특허 번호
US04284634

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