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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448050Generated: October 30, 2026

2,3-Dimethylbenzoic acid → HCID 24956422, compound

https://huagongshe.com/reaction/448050

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dimethylbenzoic acidHCID 11782—
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 24956422HCID 24956422—

Reaction Steps

In a 20 mL vial 2,3-dimethylbenzoic 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 0.85-0.91 (m, 3 H) 1.25-1.34 (m, 2 H) 1.65-1.75 (m, 2 H) 2.23 (s, 3 H) 2.27 (s, 3 H) 2.48 (s, 3 H) 4.12 (t, 2 H) 6.09-6.13 (m, 1 H) 7.07-7.14 (m, 1 H) 7.16-7.23 (m, 2 H); MS (ESI) m/z 303 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481574B2
Source datasetuspto-grants-2013_07
ORD IDord-6d49993fd0714c34bf97484dabe7e7b6
Source noteuspto-grants-2013_07