HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448048Generated: October 29, 2026
3-(Trifluoromethyl)benzoic acid → HCID 24956061, compound
https://huagongshe.com/reaction/448048
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(Trifluoromethyl)benzoic acid | HCID 9963 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 3-Butyl-2,5-dimethyl-1,3,4-thiadiazol-3-ium iodide | HCID 69187917 | — |
| Product | HCID 24956061 | HCID 24956061 | — |
Reaction Steps
In a 20 mL vial 3-(trifluoromethyl)benzoic acid (0.9 mL of 0.2 M in DMA, 1.10 equiv) was added followed by the addition of HATU (76 mg in 0.7 mL of DMA, 0.2 mmol, 1.20 equiv.), DIEA (51 mg in 0.7 mL of DMA, 0.4 mmol, 2.40 equiv.), and finally 3-butyl-2,5-dimethyl-1,3,4-thiadiazol-3-ium iodide (49 mg in 0.7 mL of DMA, 0.17 mmol, 1 equiv.). The mixture was shaken overnight at room temperature and then concentrated in vacuo. The resulting residue was taken up in 1:1 DMSO/MeOH and purified by reverse phase HPLC using a method analogous to that described in Example 53 to provide the title compound. 1H NMR (500 MHz, DMSO-d6/D2O) δ ppm 0.92 (t, 3H) 1.30-1.39 (m, 2 H) 1.72-1.80 (m, 2 H) 2.49-2.51 (m, 3 H) 4.30 (t, 2 H) 6.83-6.85 (m, 1 H) 7.69-7.74 (m, 1 H) 7.80-7.89 (m, 1 H) 8.25-8.30 (m, 1 H) 8.32-8.36 (m, 1H); MS (ESI) m/z 343 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481574B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-dcaec81bac4443588832596ef67fb46b |
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| Source note | uspto-grants-2013_07 |
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