HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378287Generated: October 25, 2026
Triethylamine → N-(2,6-bis-methylamino-pyrimidin-4-yl)-4-chloro-benzenesulfonamide
https://huagongshe.com/reaction/378287
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | 4-chloro-N-(6-chloro-2-methylamino-pyrimidin-4-yl)-benzenesulfonamide | HCID 19353555 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(2,6-bis-methylamino-pyrimidin-4-yl)-4-chloro-benzenesulfonamide | HCID 17774528 | 45% |
Reaction Steps
0.62 g (0.0019 mol) of 4-chloro-N-(6-chloro-2-methylamino-pyrimidin-4-yl)-benzenesulfonamide was dissolved in 10 ml of ethanol, treated with 1.67 g (0.025 mol) of methylamine hydrochloride and 6.2 ml (0.044 mol) of triethylamine and stirred in an autoclave at 140° C. for 18 hours. The mixture was freed completely from solvent, the residue was partitioned in ethyl acetate/water and the insoluble constituents were filtered off under suction. The filter cake was recrystallized in methanol/diethyl ether. There was obtained 0.28 g (45%) of N-(2,6-bis-methylamino-pyrimidin-4-yl)-4-chloro-benzenesulfonamide as white crystals; m.p. 272-273° 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-b19d8bc201604946b3d9f6e15227402e |
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| Source note | uspto-grants-2000_02 |
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