HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538644Generated: October 29, 2026
Dimethylformamide → US10570125, Example 1
https://huagongshe.com/reaction/538644
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Methyl-2-(4,4,4-trifluorobutane-1-sulfonyl)-propionic acid | HCID 59253161 | — |
| Reactant | 2-(5-Aminoisoxazol-3-yl)-2-methylpropanenitrile | HCID 66876608 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | US10570125, Example 1 | HCID 86297381 | 52.4% |
Reaction Steps
To 100 mg (0.38 mmol) of 2-methyl-2-(4,4,4-trifluoro-butane-1-sulfonyl)-propionic acid (intermediate 5) in toluene (4.07 mL) are added 55.3 μL (0.76 mmol) thionyl chloride and 3.10 μL (0.04 mmol) DMF. The solution is stirred at reflux for 1 h. In a second flask 78.7 μL (0.46 mmol) DIPEA are added to 63.4 mg (0.42 mmol) of 2-(5-amino-isoxazol-3-yl)-2-methyl-propionitrile (intermediate 7) in toluene (2.03 mL). The mixture is stirred at RT for 5 min, then added to the acid chloride and stirring is continued at RT for 16 h. The reaction mixture is purified by HPLC-MS to afford 78.7 mg of N-[3-(cyano-dimethyl-methyl)-isoxazol-5-yl]-2-methyl-2-(4,4,4-trifluoro-butane-1-sulfonyl)-propionamide. Yield: 52%; ESI-MS: 396 [M+H]+; HPLC (Rt): 1.14 min (method G); 1H-NMR (400 MHz, DMSO-d6): 1.68 (s, 6H), 1.70 (s, 6H), 1.86-1.91 (m, 2H), 2.47-2.52 (m, 2H), 3.34-3.40 (m, 2H), 6.57 (s, 1H), 11.64 (s, 1H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865744B1 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-9a44e784f46346aabbdbc4c7feb4fe99 |
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| Source note | uspto-grants-2014_10 |
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