HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039733Generated: October 29, 2026
Benzenesulfonic Acid → HCID 178429969, compound
https://huagongshe.com/reaction/2039733
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenesulfonic Acid | HCID 7371 | — |
| Reactant | Nilotinib | HCID 644241 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178429969 | HCID 178429969 | — |
Reaction Steps
To a 1 L round-bottom flask equipped with a mechanical stirrer, a thermometer, and a condenser, 4 g of 4-methyl-N-[3-(4-methyl-imidazol-1-yl)-5-trifluoromethyl-phenyl]-3-(4-pyridin-3-yl-pyrimidin-2-ylamino)-benzamide free base and 500 mL of ethyl acetate were charged. The slurry was stirred and heated to 76° C. (reflux) and held at that temperature for 40 minutes. To the resulting clear solution, 7.5 mL of 1 M benzene sulfonic acid solution (in ethyl acetate) was added. The mixture was stirred at 76° C. for 5 hours, cooled down to room temperature by natural cooling (cooling rate ˜0.5° C./min) and held at room temperature for ˜1 hour. The solid was collected by filtration and was dried at 50-55° C./10-20 torr for 8-16 hours to obtain 4-methyl-N-[3-(4-methyl-imidazol-1-yl)-5-trifluoromethyl-phenyl]-3-(4-pyridin-3-yl-pyrimidin-2-ylamino)-benzamide mono benzyl sulfonate salt as a yellowish solid. Melting point=˜260° C.; x-ray diffraction pattern showing maxima at 2θ=6.5°, 7.8°, 9.4°, 10.4°, 13.7°, 17.0°, 17.5°, 17.9°, 18.8°, 212°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08580806B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-b59be228b4f544f398e3bf1190a8e5af |
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| Source note | uspto-grants-2013_11 |
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