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5-[4-(4-(2-Amino-2-methoxycarbonylethyl) phenoxy)benzilidene]thiazolidin-2,4-dione → 5-[4-(4-(2-Amino-2-methoxycarbonylethyl)phenoxy)benzyl]thiazolidin-2,4-dione

HRID 1007286
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HRID 1007286 반응식
[NH2:1][CH:2]([C:25]([O:27][CH3:28])=[O:26])[CH2:3][C:4]1[CH:24]=[CH:23][C:7]([O:8][C:9]2[CH:22]=[CH:21][C:12]([CH:13]=[C:14]3[S:18][C:17](=[O:19])[NH:16][C:15]3=[O:20])=[CH:11][CH:10]=2)=[CH:6][CH:5]=1>CO>[NH2:1][CH:2]([C:25]([O:27][CH3:28])=[O:26])[CH2:3][C:4]1[CH:24]=[CH:23][C:7]([O:8][C:9]2[CH:22]=[CH:21][C:12]([CH2:13][CH:14]3[S:18][C:17](=[O:19])[NH:16][C:15]3=[O:20])=[CH:11][CH:10]=2)=[CH:6][CH:5]=1
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참가 물질

3

반응물 1

HCID 730387895-[4-(4-(2-Amino-2-methoxycarbonylethyl) phenoxy)benzilidene]thiazolidin-2,4-dione

생성물 1

HCID 99308555-[4-(4-(2-Amino-2-methoxycarbonylethyl)phenoxy)benzyl]thiazolidin-2,4-dione

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 5-[4-(4-(2-amino-2-methoxycarbonylethyl)phenoxy)benzilidene]thiazolidin-2,4-dione (0.7 g, 1.6 mmol) in methanol (20 ml) dry Pd/C (0.15 g) was added. After hydrogenating at 60 psi at 40° C. over night, the solution was filtered with Celite and evaporated under reduced pressure to yield quantitatively the title compound. This compound did not show melting in DSC but changes to black colour, in capillary and shrinks at 97-133° C. Compound 2.

후처리

  • waitAfter hydrogenating at 60 psi at 40° C. over night
  • filtrationthe solution was filtered with Celite
  • customevaporated under reduced pressure
  • 출처 및 근거

    ORD 기록
    ord-a4f25d81bbfa44399d6a81a0f8d0f009
    출처 데이터셋
    uspto-grants-2004_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06794401B2

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