Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | HCID 14720686 | HCID 14720686 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54523503 | HCID 54523503 | 49.3% |
Reaction Steps
0.53 g of N-(1,3-dimethyl-4-ethoxycarbonyl-5-pyrazolesulfonyl)-N'-(4,6-dimethyl-2-pyrimidinyl)-thiourea is suspended in 30 ml of methanol, followed by adding dropwise 0.21 g of bromine while stirring at 0° C. The suspension is stirred at the same temperature for 30 minutes and then at room temperature for 30 minutes. Then the precipitating crystals are filtered and washed with methanol. Recrystallization of the crystals from acetonitrile yields 0.26 g of the title compound as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04872901 |
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| Source dataset | uspto-grants-1989_10 |
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| ORD ID | ord-598cb81fd0b54a3eb271320b7cd01d43 |
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| Source note | uspto-grants-1989_10 |
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