HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372979Generated: October 30, 2026
4-Chloro-2-(methylthio)pyrimidine-5-carboxylic acid ethyl ester → HCID 135670794, compound
https://huagongshe.com/reaction/372979
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chloro-2-(methylthio)pyrimidine-5-carboxylic acid ethyl ester | HCID 80008 | — |
| Reactant | HCID 12535786 | HCID 12535786 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 135670794 | HCID 135670794 | 235.6% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05162316 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-d49801bf9dfd482bb8ec202ddf9b15bd |
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| Source note | uspto-grants-1992_11 |
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