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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448059Generated: October 30, 2026

2,5-Dichlorobenzoic acid → HCID 24956778, compound

https://huagongshe.com/reaction/448059

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-Dichlorobenzoic acidHCID 5784—
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 24956778HCID 24956778—

Reaction Steps

In a 20 mL vial 2,5-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 0.89 (t, 3 H) 1.27-1.35 (m, 2 H) 1.67-1.76 (m, 2 H) 2.50 (s, 3 H) 4.16 (t, 2 H) 6.25 (s, 1 H) 7.46-7.53 (m, 2 H) 7.55-7.57 (m, 1 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-c062576e4fe64c038984b187b08aef02
Source noteuspto-grants-2013_07