HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378292Generated: November 1, 2026
4,6-Dichloro-n-methylpyrimidin-2-amine → HCID 17774521, compound
https://huagongshe.com/reaction/378292
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4,6-Dichloro-n-methylpyrimidin-2-amine | HCID 259880 | — |
| Reactant | HCID 12228336 | HCID 12228336 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 17774521 | HCID 17774521 | 46.1% |
Reaction Steps
5.38 g (0.0275 mol) of benzenesulfonamide potassium salt and 2.45 g (0.0138 mol) of 2-methylamino-4,6-dichloro-pyrimidine were suspended in 22 ml of 1-methyl-2-pyrrolidone and stirred at 150° C. for 24 hours. The solvent was removed in a high vacuum and the residue was suspended in 250 ml of water. The mixture was extracted three times with 100 ml of ethyl acetate each time and the combined organic phases were washed with 200 ml of saturated NaHCO3. The combined aqueous phases were made acid with 3N HCl and the precipitate which thereby separated was filtered off under suction. It was chromatographed on silica gel with dichloromethane/methanol 99:1→98:2. The yellowish crystals obtained after the chromatography were suspended in 70 ml of 1N NaOH, the suspension was filtered and the clear filtrate was adjusted to pH 3.5 with 1N HCl. The precipitate which thereby separated was isolated and dried. There were obtained 1.9 g (46%) of N-(2-methylamino-6-chloro-pyrimidin-4-yl)-benzenesulfonamide as colorless crystals; m.p.: 186-187° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06030976 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-2ca9d83fd5f3443fa8194cebddfd83ee |
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| Source note | uspto-grants-2000_02 |
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