HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378272Generated: October 30, 2026
Trimethylamine → 4-amino-N-(2-ethylamino-6-methylamino-pyrimidin-4-yl)-benzenesulfonamide
https://huagongshe.com/reaction/378272
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylamine | HCID 1146 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | 4-amino-N-(6-chloro-2-ethylamino-pyrimidin-4-yl)-benzenesulfonamide | HCID 10830093 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-amino-N-(2-ethylamino-6-methylamino-pyrimidin-4-yl)-benzenesulfonamide | HCID 10710972 | 54% |
Reaction Steps
0.1 g (0.00031 mol) of 4-amino-N-(6-chloro-2-ethylamino-pyrimidin-4-yl)-benzenesulfonamide was dissolved in 20 ml of ethanol and stirred with 0.6 ml (0.0043 mol) of trimethylamine and 0.1 g (0.0015 mol) of methylamine hydrochloride in an autoclave at 130° C. for 4 hours. The reaction mixture was freed from solvent, the residue was suspended in 5 ml of ethanol and treated in an ultrasound bath for 15 minutes. The precipitate was filtered off, dissolved in 150 ml of 1N NaOH and filtered. The filtrate was adjusted to pH 6 with 0.1N HCl. The precipitate was filtered off under suction, washed with water and dried. There was obtained 0.053 g (54%) of 4-amino-N-(2-ethylamino-6-methylamino-pyrimidin-4-yl)-benzenesulfonamide as beige crystals; m.p.: 261-263° 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-2e4f447117ae4b1f96b12df214385e9c |
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| Source note | uspto-grants-2000_02 |
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