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4-{2-[4-(3-Benzyloxypropoxy)phenyl]ethyl}-3-(2,3,4,6-tetra-O-pivaloyl-beta-D-glucopyranosyloxy)-1H-pyrazolo-[3,4-b]pyridine → HCID 67340558, 화합물

HRID 2223955
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HRID 2223955 반응식
C([O:8][CH2:9][CH2:10][CH2:11][O:12][C:13]1[CH:18]=[CH:17][C:16]([CH2:19][CH2:20][C:21]2[CH:26]=[CH:25][N:24]=[C:23]3[NH:27][N:28]=[C:29]([O:30][C@@H:31]4[O:57][C@H:56]([CH2:58][O:59][C:60](=[O:65])[C:61]([CH3:64])([CH3:63])[CH3:62])[C@@H:48]([O:49][C:50](=[O:55])[C:51]([CH3:54])([CH3:53])[CH3:52])[C@H:40]([O:41][C:42](=[O:47])[C:43]([CH3:46])([CH3:45])[CH3:44])[C@H:32]4[O:33][C:34](=[O:39])[C:35]([CH3:38])([CH3:37])[CH3:36])[C:22]=23)=[CH:15][CH:14]=1)C1C=CC=CC=1>O1CCCC1.CO.[C].[Pd]>[OH:8][CH2:9][CH2:10][CH2:11][O:12][C:13]1[CH:14]=[CH:15][C:16]([CH2:19][CH2:20][C:21]2[CH:26]=[CH:25][N:24]=[C:23]3[NH:27][N:28]=[C:29]([O:30][C@@H:31]4[O:57][C@H:56]([CH2:58][O:59][C:60](=[O:65])[C:61]([CH3:64])([CH3:63])[CH3:62])[C@@H:48]([O:49][C:50](=[O:55])[C:51]([CH3:52])([CH3:53])[CH3:54])[C@H:40]([O:41][C:42](=[O:47])[C:43]([CH3:46])([CH3:45])[CH3:44])[C@H:32]4[O:33][C:34](=[O:39])[C:35]([CH3:36])([CH3:37])[CH3:38])[C:22]=23)=[CH:17][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 866143864-{2-[4-(3-Benzyloxypropoxy)phenyl]ethyl}-3-(2,3,4,6-tetra-O-pivaloyl-beta-D-glucopyranosyloxy)-1H-pyrazolo-[3,4-b]pyridine

생성물 1

HCID 67340558HCID 67340558, 화합물수율 100%

시약·촉매·용매 3

HCID 178418390HCID 178418390, 화합물촉매HCID 887Methanol용매HCID 8028
Tetrahydrofuran
용매

실험 절차

4-{2-[4-(3-Benzyloxypropoxy)phenyl]ethyl}-3-(2,3,4,6-tetra-O-pivaloyl-β-D-glucopyranosyloxy)-1H-pyrazolo-[3,4-b]pyridine (0.4 g) was dissolved in a mixed solvent of tetrahydrofuran (6 mL) and methanol (6 mL). To the solution was added 10% palladium-carbon powder (160 mg), and the mixture was stirred at room temperature under a hydrogen atmosphere for 3 hours. The insoluble material was removed by filtration, and the filtrate was concentrated under reduced pressure to give the title compound (0.36 g).

후처리

  1. customThe insoluble material was removed by filtration
  2. concentrationthe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-d0f271824ce34b7c8bb9ae1f0f8e3547
출처 데이터셋
uspto-grants-2008_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07375113B2

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