Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178502003 | HCID 178502003 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178502002 | HCID 178502002 | — |
Reaction Steps
150 g of methyl 2-amino-6-[(p-tolylsulfonyl)oxy]-4-pyrimidinecarbamate-3-oxide are suspended in 2 l of methylene chloride and 2 l of water while stirring. After cooling to 0°-5°, 50 ml of methyl chloroformate are added thereto. After stirring vigorously for about 10 minutes, the mixture is adjusted to a pH of 7-7.5 with about 150 g of sodium bicarbonate. The mixture is subsequently stirred at 0°-5° for a further 3 hours. The organic phase is separated and the aqueous phase is extracted with 1 l of methylene chloride. The combined organic phases are washed twice with 1 l of water each time, dried over sodium sulphate and evaporated in vacuo. There is obtained crude dimethyl 6-[(p-tolylsulfonyl)oxy]-2,4-pyrimidinedicarbamate-3-oxide which is used in the next step (a pure product of melting point 178°-180° can be obtained by digestion with ethyl acetate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04549019 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-934934e0a8124027b775ea22c6013d55 |
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| Source note | uspto-grants-1985_10 |
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