Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Amino-4,6-dimethoxy-1,3,5-triazine | HCID 27840 | — |
| Reactant | dimethyl N-(2-biphenylylsulfonyl)carbonimidodithioate | HCID 13422024 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178494236 | HCID 178494236 | 81.4% |
Reaction Steps
15.6 g of 2-amino-4,6-dimethoxy-1,3,5-triazine were suspended in 300 ml of dimethylformamide, and 4 g of sodium hydride (oily, 60%) were added to the suspension. The mixture was stirred at room temperature for 1 hour. Furthermore, 33.7 g of dimethyl N-(2-biphenylylsulfonyl)carbonimidodithioate were added, and the mixture was stirred at room temperature for a day and night. The reaction mixture was poured into 2 liters of water and filtered. The filtrate was made weakly acidic to precipitate white crystals. The crystals were collected by filtration and recrystallized from ethanol to give 36.2 g of 1-(2-biphenylylsulfonyl) 3-(4,6-dimethoxy-1,3,5-triazin-2-yl) 2-methylisothiourea (compound No. II-1), the same compound as obtained in Example 5. The melting point of the product was 135° to 137° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04568381 |
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| Source dataset | uspto-grants-1986_02 |
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| ORD ID | ord-caffc1f0f27246e993808c5090fda031 |
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| Source note | uspto-grants-1986_02 |
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