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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448061Generated: October 30, 2026

3,5-Dichlorobenzoic acid → HCID 24956780, compound

https://huagongshe.com/reaction/448061

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dichlorobenzoic acidHCID 5811—
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 24956780HCID 24956780—

Reaction Steps

In a 20 mL vial 3,5-dichlorobenzoic 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, 3 H) 1.28-1.37 (m, 2 H) 1.71-1.82 (m, 2 H) 2.47-2.53 (m, 3 H) 4.29 (t, 2 H) 6.83 (s, 1 H) 7.73 (s, 1 H) 8.06 (s, 2 H); MS (ESI) m/z 343 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481574B2
Source datasetuspto-grants-2013_07
ORD IDord-5a106a5c50e341f4b271667c191c6259
Source noteuspto-grants-2013_07