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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448046Generated: October 30, 2026

3-Bromobenzoic acid → HCID 24956059, compound

https://huagongshe.com/reaction/448046

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromobenzoic acidHCID 11456—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant3-Butyl-2,5-dimethyl-1,3,4-thiadiazol-3-ium iodideHCID 69187917—
ProductHCID 24956059HCID 24956059—

Reaction Steps

In a 20 mL vial 3-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 0.86-0.96 (m, 3 H) 1.27-1.41 (m, 2 H) 1.69-1.78 (m, 2 H) 2.47-2.49 (m, 3 H) 4.29 (t, 2 H) 6.77 (s, 1 H) 7.36-7.48 (m, 1 H) 7.64-7.70 (m, 1 H) 7.98-8.04 (m, 1 H) 8.12-8.19 (m, 1 H); MS (ESI) m/z 353 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481574B2
Source datasetuspto-grants-2013_07
ORD IDord-d65a3a5e2ec8474c9d5fca29c7aa784c
Source noteuspto-grants-2013_07