Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Sulfur | HCID 5362487 | — |
| Reactant | HCID 178418551 | HCID 178418551 | — |
| Product | HCID 20183313 | HCID 20183313 | — |
Reaction Steps
A mixture of methyl 1,6-dihydro-4-methyl-6-(3-nitrophenyl)-2-phenyl-5-pyrimidinecarboxylate (0.5 g) and sulfur powder (0.046 g) was heated at 150° C. for 1 hour. After cooling, the mixture was dissolved in chloroform and filtered. The filtrate was evaporated under reduced pressure to give a crystal of methyl 6-methyl-4-(3-nitrophenyl)-2-phenyl-5-pyridinecarboxylate (0.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04698340 |
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| Source dataset | uspto-grants-1987_10 |
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| ORD ID | ord-927a60651f6e47d38a89f16b60d4c9bf |
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| Source note | uspto-grants-1987_10 |
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