Process for producing trichloropyrimidine compound
A process for producing a trichloropyrimidine compound represented by the formula (2): wherein R represents a hydrogen atom etc., comprising reacting a dihydroxypyrimidine compound represented by the formula (1): wherein R represents the same meaning as above, with sulfuryl chloride and at least one chlorinating agent selected from the group consisting of hydrogen chloride, thionyl chloride, phosgene, phosphorus oxychloride, phosphorus pentachloride and phosphorus trichloride in the presence of an organic base.
1. A process for producing a trichloropyrimidine compound represented by the formula (2):
wherein R represents a hydrogen atom; a halogen atom; a mercapto group; a cyano group; a nitro group; an alkyl group which may be substituted with at least one substituent selected from the group consisting of a halogen atom, a C3-C6 cycloalkyl group, a C6-C14 aryl group, a C3-C8 heteroaryl group, a C1-C3 alkoxy group, a C1-C3 alkylthio group, a C6-C14 arylthio group, a cyano group, a nitro group, a C2-C14 disubstituted amino group and a C2-C14 disubstituted carbamoyl group; an alkoxy group; an alkenyl group; an alkynyl group; an aryl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a C2-C4 alkenyl group, a C5-C6 cycloalkyl group, a halogen atom, a C1-C3 alkoxy group, a C2-C4 alkynyl group, a C2-C14 disubstituted amino group, a nitro group, a cyano group and a C2-C14 disubstituted carbamoyl group; or a heteroaryl group which may be substituted with at least one substituent selected from the group consisting of a C1-C4 alkyl group, a benzyl group, a C6-C10 aryl group, a halogen atom, a C1-C3 alkoxy group, a nitro group, a cyano group and a C2-C14 disubstituted amino group,
comprising reacting a dihydroxypyrimidine compound represented by the formula (1):
wherein R represents the same meaning as above, with sulfuryl chloride and at least one chlorinating agent selected from the group consisting of hydrogen chloride, thionyl chloride, phosgene, phosphorus oxychloride, phosphorus pentachloride and phosphorus trichloride in the presence of an organic base.
2. The process according to claim 1 , wherein the dihydroxypyrimidine compound represented by the formula (1) is reacted with sulfuryl chloride, and the obtained reaction mixture or a treated material thereof is reacted with at least one chlorinating agent selected from the group consisting of hydrogen chloride, thionyl chloride, phosgene, phosphorus oxychloride, phosphorus pentachloride and phosphorus trichloride in the presence of an organic base.
3. The process according to claim 1 , wherein the organic base is triethylamine.
4. The process according to claim 2 , wherein the reaction of the dihydroxypyrimidine compound represented by the formula (1) and sulfuryl chloride is conducted in the presence of an organic solvent.
5. The process according to claim 4 , wherein the organic solvent is chlorobenzene.
6. The process according to claim 1 , wherein the chlorinating agent is phosphorus oxychloride.
7. The process according to claim 1 , wherein R is a hydrogen atom.
8. The process according to claim 2 , wherein the organic base is triethylamine.
9. The process according to claim 2 , wherein the chlorinating agent is phosphorus oxychloride.
10. The process according to claim 2 , wherein R is a hydrogen atom.