Phosphorus oxychloride → HCID 57468611, compound
Reaction equation
[CH2:1]([O:3][C:4]1[CH:5]=[C:6]([C:14]2[CH:19]=[C:18]([C:20]([F:23])([F:22])[F:21])[NH:17][C:16](=O)[N:15]=2)[CH:7]=[CH:8][C:9]=1[C:10]([F:13])([F:12])[F:11])[CH3:2].P(Cl)(Cl)([Cl:27])=O>>[Cl:27][C:16]1[N:15]=[C:14]([C:6]2[CH:7]=[CH:8][C:9]([C:10]([F:13])([F:12])[F:11])=[C:4]([O:3][CH2:1][CH3:2])[CH:5]=2)[CH:19]=[C:18]([C:20]([F:23])([F:22])[F:21])[N:17]=1Participants
3
Procedure
The title compound was prepared from 4-(3-ethoxy-4-trifluoromethyl-phenyl)-6-trifluoromethyl-1H-pyrimidin-2-one (3.74 g, 10.6 mmol) and phosphoryl chloride (35 mL) according to the general procedure I. Obtained as a light brown solid. MS (EI) 370.0 [(M)+]; mp 89° C.
Workup
- customObtained as a light brown solid
Sources & evidence
- ORD record
- ord-fcb40faede494d2bba45a517b8acc09b
- Source dataset
- uspto-grants-2010_01
- Patent number
- US07642264B2
Reaction notes
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