HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448047Generated: October 29, 2026
4-Bromobenzoic acid → HCID 24956060, compound
https://huagongshe.com/reaction/448047
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromobenzoic acid | HCID 11464 | — |
| 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 24956060 | HCID 24956060 | — |
Reaction Steps
In a 20 mL vial 4-bromobenzoic 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 0.85-0.94 (m, 3 H) 1.28-1.39 (m, 2 H) 1.67-1.80 (m, 2 H) 2.49 (s, 3 H) 4.20-4.23 (m, 2 H) 6.70 (m, 1 H) 7.64 (d, 2 H) 7.94 (d, 2 H); MS (ESI) m/z 353 (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-ff04103f59204dee94a61cecef7175f1 |
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| Source note | uspto-grants-2013_07 |
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