HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → methyl N-(4,6-dimethylpyrimidin-2-yl)-N'-(2-phenylphenyl)sulfonylcarbamimidothioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Amino-4,6-dimethyl pyrimidine | HCID 13021 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | dimethyl N-(2-biphenylylsulfonyl)carbonimidodithioate | HCID 13422024 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | methyl N-(4,6-dimethylpyrimidin-2-yl)-N'-(2-phenylphenyl)sulfonylcarbamimidothioate | HCID 178503865 | 70.9% |
Reaction Steps
12.3 g of 2-amino-4,6-dimethylpyrimidine was suspended in 300 ml of dimethylformamide, and 4 g of sodium hydroxide (oily 60%) was added. The mixture was stirred at room temperature for 1 hour. Furthermore, 33.7 g of dimethyl N-(2-biphenylylsulfonyl)carbonimidodithioate was 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. When the filtrate was made weakly acidic, white crystals precipitated. The crystals were collected by filtration, and recrystallized from ethanol to give 29.2 g of the desired 1-(2-biphenylylsulfonyl)3-(4,6-dimethylpyrimidin-2-yl)2-methylisothiourea of the following formula, mp. 154°-157° C.: ##STR18##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04559079 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-67a028b9013c4937aae94ff670b902ae |
| Source note | uspto-grants-1985_12 |