Piperidine → HCID 86675361, 화합물

HRID 446059

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HRID 446059 반응식
[I:1][C:2]1[CH:3]=[C:4]([C:8]2[O:12][C:11]([CH:13]=O)=[CH:10][CH:9]=2)[CH:5]=[CH:6][CH:7]=1.[CH2:15]([O:17][C:18](=[O:27])[CH2:19][N:20]1[C:24](=[O:25])[CH2:23][NH:22][C:21]1=[S:26])[CH3:16].N1CCCCC1>ClCCl>[CH2:15]([O:17][C:18](=[O:27])[CH2:19][N:20]1[C:24](=[O:25])/[C:23](=[CH:13]/[C:11]2[O:12][C:8]([C:4]3[CH:5]=[CH:6][CH:7]=[C:2]([I:1])[CH:3]=3)=[CH:9][CH:10]=2)/[NH:22][C:21]1=[S:26])[CH3:16]

참가 물질

5

반응물 3

HCID 8082PiperidineHCID 43155822HCID 43155822, 화합물HCID 43995697Ethyl-2-(5-oxo-2-thioxoimidazolidin-1-yl)acetate

생성물 1

HCID 86675361HCID 86675361, 화합물수율 43.6%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
25 °C

실험 절차

5-(3-Iodophenyl)furan-2-carbaldehyde (30 mg, 0.1 mmol) synthesized by the same method as in Example 1 and ethyl-2-(5-oxo-2-thioxoimidazolidin-1-yl)acetate (20 mg, 0.1 mmol) were dissolved in dichloromethane (7 mL), piperidine (20 μL) was added thereto, and the mixture was stirred at room temperature (25° C.) overnight. After the reaction was completed the solvent was removed by evaporation under reduced pressure, and the residue was subjected to silica gel column chromatography using ethyl acetate/hexane (3/7 (volume ratio)) as an eluent, to give compound 2 in a yield of 21 mg (yield 43.6%).

후처리

  1. customwas removed by evaporation under reduced pressure

출처 및 근거

ORD 기록
ord-8b5708c1b379492382885c12243bcee2
출처 데이터셋
uspto-grants-2013_07
특허 번호
US08476449B2

연결된 노트

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