HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165740Generated: October 26, 2026
Formaldehyde → 4,6-Dimethyl-2-(4-tolylsulfonylmethylamino)pyrimidine
https://huagongshe.com/reaction/2165740
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 2-Amino-4,6-dimethyl pyrimidine | HCID 13021 | — |
| Reactant | m-Toluenesulfonic acid | HCID 105362 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4,6-Dimethyl-2-(4-tolylsulfonylmethylamino)pyrimidine | HCID 23043221 | — |
Reaction Steps
12.7 g (0.1 mole) of 2-amino-4,6-dimethylpyrimidine are suspended in 200 ml of water and then 9.7 g (0.1 mole) of methanesulfonic acid are stirred in to form a solution. To the stirred solution are added, in succession, 18.22 g (0.1 mole) of toluene-3-sulfonic acid, sodium salt, and 9.4 g (0.11 mole) of aqueous 35% formaldehyde. The mixture is stirred for 2 hours at room temperature and for another 30 minute at 90° C. The colourless precipitate is filtered with suction after cooling and dried. Melting point: 191°-194° C. Yield: 25 g (86% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04940792 |
|---|
| Source dataset | uspto-grants-1990_07 |
|---|
| ORD ID | ord-2837409a102245318abf35a40b59479a |
|---|
| Source note | uspto-grants-1990_07 |
|---|