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5-Methoxy-3-phenyl-2-(pyridin-3-yl)-1H-inden-1-one → 5-Hydroxy-3-phenyl-2-(pyridin-3-yl)-1H-inden-1-one

HRID 331390
Notes
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Reaction equation

HRID 331390 reaction equation
C[O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[C:8](=[O:12])[C:7]([C:13]1[CH:14]=[N:15][CH:16]=[CH:17][CH:18]=1)=[C:6]2[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.FC1C=C(C2C3C(=CC=C(OC)C=3)C(=O)C=2C2C=NC=CC=2)C=C(F)C=1>>[OH:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[C:8](=[O:12])[C:7]([C:13]1[CH:14]=[N:15][CH:16]=[CH:17][CH:18]=1)=[C:6]2[C:19]1[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 703100415-Methoxy-3-phenyl-2-(pyridin-3-yl)-1H-inden-1-oneHCID 703136143-(3,5-Difluorophenyl)-5-methoxy-2-(pyridin-3-yl)-1H-inden-1-one

Product 1

HCID 703128045-Hydroxy-3-phenyl-2-(pyridin-3-yl)-1H-inden-1-oneYield 93%

Procedure

The procedure of Step 5 of Example 128 was repeated except for using 5-methoxy-3-phenyl-2-(pyridin-3-yl)-1H-inden-1-one obtained in Step 5 as a starting material instead of 3-(3,5-difluorophenyl)-5-methoxy-2-(pyridin-3-yl)-1H-inden-1-one to obtain the title compound (93%).

Sources & evidence

ORD record
ord-7fd35b31067f4262b92a672057e47cc0
Source dataset
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08877747B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes