HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378261Generated: October 29, 2026
Ethylamine → 4-Amino-N-(2-amino-6-ethylamino-pyrimidin-4-yl)-benzenesufonamide
https://huagongshe.com/reaction/378261
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | 4-amino-N-(2-amino-6-chloro-pyrimidin-4-yl)-benzenesulfonamide | HCID 10732939 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Amino-N-(2-amino-6-ethylamino-pyrimidin-4-yl)-benzenesufonamide | HCID 10733598 | 53% |
Reaction Steps
0.50 g (0.00167 mol) of 4-amino-N-(2-amino-6-chloropyrimidin-4-yl)-benzenesufonamide and 11 ml (0.167 mol) of ethylamine were dissolved in 20 ml of ethanol and stirred 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 10 ml of 0.1N 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 0.271 g (53%) of 4-amino-N-(2-amino-6-ethylamino-pyrimidin-4-yl)-benzenesulfonamide as beige crystals; m.p. 272-274° 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-0edc4226fa484de9b7f2dc1416f466e8 |
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| Source note | uspto-grants-2000_02 |
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