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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448056Generated: October 25, 2026

3,5-Dimethoxybenzoic Acid → HCID 24956428, compound

https://huagongshe.com/reaction/448056

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dimethoxybenzoic AcidHCID 14332—
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 24956428HCID 24956428—

Reaction Steps

In a 20 mL vial 3,5-dimethoxybenzoic 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 0.87-0.97 (m, 3 H) 1.28-1.37 (m, 2 H) 1.71-1.80 (m, 2 H) 2.46-2.48 (m, 3 H) 3.77-3.83 (m, 6 H) 4.23 (t, 2 H) 6.60-6.68 (m, 2 H) 7.10-7.14 (m, 2 H); MS (ESI) m/z 335 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481574B2
Source datasetuspto-grants-2013_07
ORD IDord-069a05992a5f4d97b5128ec595a7c6b2
Source noteuspto-grants-2013_07