Methyl chloroformate → HCID 20130645, compound
Reaction equation
[Cl:1][C:2]1[CH:13]=[C:12]([F:14])[C:11]([N:15]2[C:20](=[O:21])[C:19]3[CH2:22][CH2:23][CH2:24][C:18]=3[NH:17][C:16]2=[O:25])=[CH:10][C:3]=1[C:4]([O:6][CH:7]([CH3:9])[CH3:8])=[O:5].Cl[C:27]([O:29][CH3:30])=[O:28]>>[Cl:1][C:2]1[CH:13]=[C:12]([F:14])[C:11]([N:15]2[C:20](=[O:21])[C:19]3[CH2:22][CH2:23][CH2:24][C:18]=3[N:17]([C:27]([O:29][CH3:30])=[O:28])[C:16]2=[O:25])=[CH:10][C:3]=1[C:4]([O:6][CH:7]([CH3:9])[CH3:8])=[O:5]Participants
3
Procedure
using isopropyl 2-chloro-4-fluoro-5-(1,2,4,5,6,7-hexahydro-2,4-dioxo-3H-cyclopenta[d]pyrimidin-3-yl)-benzoate and methyl chloroformate there is obtained isopropyl 2-chloro-4-fluoro-5-(1,2,4,5,6,7-hexahydro-1-methoxycarbonyl-2,4-dioxo-3H-cyclopenta[d]pyrimidin-3-yl)-benzoate, 1H-NMR (CDCl3, 400 MHz) 7.84 ppm (d, 1H), 7.35 ppm (d, 1H), 5.24 ppm (m, 1H), 4.03 ppm (s, 3H), 3.02 ppm (m, 2H), 2.79 ppm (m, 2H), 2.16 ppm, (m, 2H), 1.36 ppm (d, 6H),
Sources & evidence
- ORD record
- ord-ab3005217feb4c14b6d9c4b257657738
- Source dataset
- uspto-grants-1988_05