HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747401Generated: October 29, 2026
Dimethylformamide → HCID 12085659, compound
https://huagongshe.com/reaction/747401
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 3-[2-chloro-4-(4-chlorophenyl)-5-oxazolyl]propionate | HCID 10990225 | — |
| Reactant | HCID 178418793 | HCID 178418793 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12085659 | HCID 12085659 | — |
Reaction Steps
A mixture of methyl 2-chloro-4-(4-chlorophenyl)-5-oxazolepropionate (2.00 g), 2-mercaptopyrimidine (819 mg), anhydrous potassium carbonate (1.10 g) and N,N-dimethylformamide (10 ml) was heated to 100-110° C. and stirred for 4 hours. The reaction mixture was poured into water (100 ml) and extracted with ethyl acetate (100 ml×2). The organic layer was dried over anhydrous magnesium sulfate and then concentrated, the residue was subjected to silica gel column chromatography, and methyl 4-(4-chlorophenyl)-2-(2-pyrimidinylsulfanyl)-5-oxazolepropionate was obtained as a yellow oil (1.42 g, 57%) from an ethyl acetate-hexane (1:4, v/v)-eluted fraction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07396848B1 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-8dce50feea2246d492294b3b4f49c3d5 |
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| Source note | uspto-grants-2008_07 |
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