HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428788Generated: November 3, 2026
(2-m-Tolyl-6-(trifluoromethyl)pyridin-3-yl)methanamine → HCID 89455636, compound
https://huagongshe.com/reaction/1428788
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (2-m-Tolyl-6-(trifluoromethyl)pyridin-3-yl)methanamine | HCID 86680208 | — |
| Reactant | HCID 131732364 | HCID 131732364 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 89455636 | HCID 89455636 | 51% |
Reaction Steps
2-(N-(2-Fluoro-4-(phenoxycarbonylamino)benzyl)sulfamoylcarbamoyloxy)-2-methylpropan-1-ylium (100 mg, 0.225 mmol) was dissolved in acetonitrile. (2-m-Tolyl-6-(trifluoromethyl)pyridin-3-yl)methanamine (60 mg, 0.225 mmol) and 4-dimethylaminopyridine (27 mg) were added to the solution. The reaction mixture was stirred for overnight at 50° C. The mixture was extracted with ethyl acetate and washed with brine. Drying over magnesium sulfate, evaporation of the ethyl acetate and purification by column chromatography gave tert-butyl N-(2-fluoro-4-(3-((2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methyl)ureido)benzyl)sulfamoylcarbamate (70 mg, 51%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08937092B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-4a930dd291f7404a9a9cf9f2722421a6 |
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| Source note | uspto-grants-2015_01 |
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