(3R)-3-ethyl-7-fluoro-4-(4-hydroxybenzoyl)-1-methyl-3,4-dihydroquinoxalin-2(1H)-one → (3R)-3-ethyl-6-fluoro-4-(4-hydroxybenzoyl)-1-propyl-3,4-dihydroquinoxalin-2(1H)-one
Reaction equation
[CH2:1]([C@H:3]1[N:12]([C:13](=[O:22])[C:14]2[CH:19]=[CH:18][C:17]([O:20]C)=[CH:16][CH:15]=2)[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([F:23])[CH:10]=2)[N:5]([CH2:24][CH2:25][CH3:26])[C:4]1=[O:27])[CH3:2].C([C@H]1N(C(=O)C2C=CC(O)=CC=2)C2C(=CC(F)=CC=2)N(C)C1=O)C>>[CH2:1]([C@H:3]1[N:12]([C:13](=[O:22])[C:14]2[CH:19]=[CH:18][C:17]([OH:20])=[CH:16][CH:15]=2)[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([F:23])[CH:10]=2)[N:5]([CH2:24][CH2:25][CH3:26])[C:4]1=[O:27])[CH3:2]Participants
3
Reactant 2
Product 1
Procedure
(3R)-3-Ethyl-6-fluoro-4-(4-methoxybenzoyl)-1-propyl-3,4-dihydroquinoxalin-2(1H)-one was treated according to the procedure for the preparation of (3R)-3-ethyl-7-fluoro-4-(4-hydroxybenzoyl)-1-methyl-3,4-dihydroquinoxalin-2(1H)-one (see Example 1) to yield (3R)-3-ethyl-6-fluoro-4-(4-hydroxybenzoyl)-1-propyl-3,4-dihydroquinoxalin-2(1H)-one (81%). [α]D25=−298° (c=0.0102 G/ML, CHCl3); MS (ESI) m/z 357 ([M+H]+); MS (ESI) m/z 355 ([M−H]−); HRMS: calcd for C20H21FN2O3, 356.1536; found (ESI_FT), 357.16057.
Sources & evidence
- ORD record
- ord-84349816436942caa2955850ad316ac2
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07351709B2
Reaction notes
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