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Methyl 2-(3-acetyl-5-(benzyloxy)-1H-indazol-1-yl)acetate → Methyl 2-(3-acetyl-5-hydroxy-1H-indazol-1-yl)acetate

HRID 1527283
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HRID 1527283 반응식
[C:1]([C:4]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([O:13]CC3C=CC=CC=3)[CH:11]=2)[N:6]([CH2:21][C:22]([O:24][CH3:25])=[O:23])[N:5]=1)(=[O:3])[CH3:2]>C1COCC1.[Pd]>[C:1]([C:4]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([OH:13])[CH:11]=2)[N:6]([CH2:21][C:22]([O:24][CH3:25])=[O:23])[N:5]=1)(=[O:3])[CH3:2]
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참가 물질

4

반응물 1

HCID 68284049Methyl 2-(3-acetyl-5-(benzyloxy)-1H-indazol-1-yl)acetate

생성물 1

HCID 68283743Methyl 2-(3-acetyl-5-hydroxy-1H-indazol-1-yl)acetate

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8028Tetrahydrofuran용매

반응 조건

온도
50 °C

실험 절차

To methyl 2-(3-acetyl-5-(benzyloxy)-1H-indazol-1-yl)acetate (3.70 g, 10.9 mmol) in THF (80 mL) was added Pd/C (10%, 400 mg). The reaction mixture was stirred at 50° C. overnight under a H2 atmosphere. The reaction mixture was filtered over a pad of Celite and washed with CH2Cl2, then volatiles were evaporated to give the title compound. MS (LC/MS): 248.9 [M+H]+, 271.0 [M+Na]+; tR (HPLC conditions c): 3.36 min.

후처리

  1. filtrationThe reaction mixture was filtered over a pad of Celite
  2. washwashed with CH2Cl2
  3. customvolatiles were evaporated

출처 및 근거

ORD 기록
ord-6541c783da254b27a06a5a20a75a3d9e
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09085555B2

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