4-Chloro-2-(methylthio)pyrimidine-5-carboxylic acid ethyl ester → HCID 135670794, compound
Reaction equation
[CH2:1]([O:4][C:5]1[CH:13]=[CH:12][CH:11]=[CH:10][C:6]=1[C:7]([NH2:9])=[NH:8])[CH:2]=[CH2:3].Cl[C:15]1[C:20]([C:21](OCC)=[O:22])=[CH:19][N:18]=[C:17]([S:26][CH3:27])[N:16]=1>C(#N)C>[CH3:27][S:26][C:17]1[N:18]=[C:19]2[N:8]=[C:7]([C:6]3[CH:10]=[CH:11][CH:12]=[CH:13][C:5]=3[O:4][CH2:1][CH:2]=[CH2:3])[NH:9][C:21](=[O:22])[C:20]2=[CH:15][N:16]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 2 °C
Procedure
2-Allyloxybenzamidine (from sodium, 0.22 g, in ethanol, 100 ml, and 2 allyloxybenzamidine hydrochloride, 2.00 g) was dissolved in acetonitrile (50 ml) and the resulting cooled (2° C.) solution was added to a cooled (2° C.) solution of ethyl 4-chloro-2-methylthio-5-pyrimidine carboxylate (2.19 g) in acetonitrile (50 ml). The temperature was allowed to rise and the reaction mixture was stirred overnight at ambient temperature. The volume of the reaction mixture was reduced by evaporation under reduced pressure to yield a solid (0.96 g) which was collected. More product (0.45 g) precipitated from the filtrate. The combined products were recrystallised twice from ethanol to yield the title compound, 340 mg, m.p. 205°-206° C.
Workup
- additionwas added to
- customThe volume of the reaction mixture was reduced by evaporation under reduced pressure
Sources & evidence
- ORD record
- ord-d49801bf9dfd482bb8ec202ddf9b15bd
- Source dataset
- uspto-grants-1992_11
- Patent number
- US05162316
Reaction notes
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