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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448052Generated: October 30, 2026

3,4-Dimethylbenzoic acid → HCID 24956424, compound

https://huagongshe.com/reaction/448052

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dimethylbenzoic acidHCID 12073—
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 24956424HCID 24956424—

Reaction Steps

In a 20 mL vial 3,4-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 0.87-0.95 (m, 3 H) 1.30-1.41 (m, 2 H) 1.69-1.80 (m, 2 H) 2.23-2.32 (m, 6 H) 2.47 (s, 3 H) 4.21 (t, 2 H) 6.65 (s, 1 H) 7.15-7.27 (m, 1 H) 7.65-7.80 (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-f0eab35262254128a2d05752dba0164a
Source noteuspto-grants-2013_07