Acetic Acid → HCID 178458305, compound
Reaction equation
[OH:1][C:2]1[N:7]=[C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[O:14][CH2:15][CH2:16][CH3:17])[N:5]=[C:4]([C:18]([NH2:20])=O)[CH:3]=1.C(O)(=O)C>P(Cl)(Cl)(Cl)=O>[C:18]([C:4]1[CH:3]=[C:2]([OH:1])[N:7]=[C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[O:14][CH2:15][CH2:16][CH3:17])[N:5]=1)#[N:20]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A stirred solution of 6-hydroxy-2-(2-propoxyphenyl)pyrimidine-4-carboxamide (0.50 g) in phosphoryl chloride (16 ml) was heated under reflux for 4 hours and then the reaction mixture was evaporated under reduced pressure to remove excess phosphoryl chloride. Water was added to the residue, which was extracted with chloroform (3×20 ml). The combined extracts were washed with water, dried (magnesium sulfate) and evaporated under reduced pressure to yield an oil which was heated on a steam bath with glacial acetic acid (15 ml) for 4 hours. The cooled reaction mixture was evaporated under reduced pressure to yield a crude product which was combined with further product similarly prepared from 6-hydroxy-2-(2-propoxyphenyl)-pyrimidine-4-carboxamide (0.82 g) and phosphoryl chloride (25 ml). The combined products were eluted from silica with ether:chloroform (9:1) and fractions containing product were combined and evaporated under reduced pressure to yield the title compound, 0.31 g, m.p. 135°-6° C. (from isopropanol/ether).
Workup
- temperatureunder reflux for 4 hours
- customthe reaction mixture was evaporated under reduced pressure
- customto remove excess phosphoryl chloride
- additionWater was added to the residue, which
- extractionwas extracted with chloroform (3×20 ml)
- washThe combined extracts were washed with water
- dry with materialdried (magnesium sulfate)
- customevaporated under reduced pressure
- customto yield an oil which
- customThe cooled reaction mixture
- customwas evaporated under reduced pressure
- customto yield a crude product which
- washThe combined products were eluted from silica with ether:chloroform (9:1) and fractions
- additioncontaining product
- customevaporated under reduced pressure
Sources & evidence
- ORD record
- ord-db8c276137b343eb89f21168b963a521
- Source dataset
- uspto-grants-1999_02
- Patent number
- US05874440
Reaction notes
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