Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | HCID 12202399 | HCID 12202399 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 12202410 | HCID 12202410 | — |
Reaction Steps
To a solution of 450 mg of 1-methyl-4-(o-chlorophenyl)-1,2-dihydrothieno[2,3-d]pyrimidin-2-one in 11 ml of chloroform is added dropwise 0.66 g of sulfuryl chloride. After stirring the reaction mixture for 7 hours at 50°C, the reaction mixture is neutralized with aqueous ammonia, then extracted with chloroform. The chloroform extracts are washed with water, dried and evaporated under reduced pressure to a residue to give crystals, which are recrystallized from ethanol-ether to give 1-methyl-4-(o-chlorophenyl)-6-chloro-1,2-dihydrothieno[2,3-d]pyrimidin-2-one as crystals having a melting point of 164° - 166°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03957783 |
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| Source dataset | uspto-grants-1976_05 |
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| ORD ID | ord-53f0a2bf76eb45f098f868371df8235e |
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| Source note | uspto-grants-1976_05 |
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