Phosphorus pentachloride → HCID 14278970, compound
Reaction equation
[O:1]=[C:2]1[N:7]2[CH:8]=[C:9]([O:20][CH2:21][C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)[C:10]([O:12][CH2:13][C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)=[CH:11][C:6]2=[N:5][CH:4]=[C:3]1[C:28]([OH:30])=O.P(Cl)(Cl)(Cl)(Cl)[Cl:32]>ClCCl>[O:1]=[C:2]1[N:7]2[CH:8]=[C:9]([O:20][CH2:21][C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)[C:10]([O:12][CH2:13][C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)=[CH:11][C:6]2=[N:5][CH:4]=[C:3]1[C:28]([Cl:32])=[O:30]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a suspension of 4-oxo-7,8-bis(phenylmethoxy)-4H-pyrido[1,2-a]pyrimidine-3-carboxylic acid (1.21 g, 3.0 mmol) in 30 ml of dichloromethane was added 0.69 g (3.3 mmol) of phosphorous pentachloride at 0° C. After stirring for 90 minutes, the solid was filtered off, washed with dichloromethane and dried in vacuo. Yield: 0.91 g; melting point 152.4° C.
Workup
- filtrationthe solid was filtered off
- washwashed with dichloromethane
- customdried in vacuo
Sources & evidence
- ORD record
- ord-3061bf74d64d4c8bad1e5922c3e1e8f6
- Source dataset
- uspto-grants-1988_10
- Patent number
- US04777252
Reaction notes
Loading…