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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-[2-Benzyloxy-5-(5-methyl-7-nitroindan-4-yloxy)benzylidene]tetrahydropyran → 4-(7-Amino-5-methylindan-4-yloxy)-2-(tetrahydropyran-4-yl methyl)phenol

HRID 1766653
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HRID 1766653 반응식
C([O:8][C:9]1[CH:21]=[CH:20][C:19]([O:22][C:23]2[C:31]([CH3:32])=[CH:30][C:29]([N+:33]([O-])=O)=[C:28]3[C:24]=2[CH2:25][CH2:26][CH2:27]3)=[CH:18][C:10]=1[CH:11]=[C:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1)C1C=CC=CC=1.[H][H]>C(O)C.C(OCC)(=O)C.[Pd]>[NH2:33][C:29]1[CH:30]=[C:31]([CH3:32])[C:23]([O:22][C:19]2[CH:20]=[CH:21][C:9]([OH:8])=[C:10]([CH2:11][CH:12]3[CH2:17][CH2:16][O:15][CH2:14][CH2:13]3)[CH:18]=2)=[C:24]2[C:28]=1[CH2:27][CH2:26][CH2:25]2
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참가 물질

6

반응물 2

HCID 211105754-[2-Benzyloxy-5-(5-methyl-7-nitroindan-4-yloxy)benzylidene]tetrahydropyranHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 230311814-(7-Amino-5-methylindan-4-yloxy)-2-(tetrahydropyran-4-yl methyl)phenol수율 80%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 702Ethanol용매
HCID 8857
Ethyl Acetate
용매

실험 절차

4-[2-Benzyloxy-5-(5-methyl-7-nitroindan-4-yloxy) benzylidene]tetrahydropyran (230 mg) was dissolved in ethanol (10 mL) and ethyl acetate (2 mL). After adding 10% Pd/C (50 mg) under ice-cooling, the mixture was stirred at room temperature under an atmospheric pressure of hydrogen for 24 hours. The insoluble material was removed by filtration. The filtrate was evaporated under reduced pressure to dryness. The residue was purified by column chromatography on silica gel (eluent: exane/ethyl acetate) to give the title compound (138 mg).

후처리

  1. temperaturecooling
  2. customThe insoluble material was removed by filtration
  3. customThe filtrate was evaporated under reduced pressure to dryness
  4. customThe residue was purified by column chromatography on silica gel (eluent: exane/ethyl acetate)

출처 및 근거

ORD 기록
ord-de6cd3345990483bb65b3dad9d721862
출처 데이터셋
uspto-grants-2007_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07230031B2

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