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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448055Generated: October 30, 2026

2,5-Dimethoxybenzoic acid → HCID 24956427, compound

https://huagongshe.com/reaction/448055

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-Dimethoxybenzoic acidHCID 76027—
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 24956427HCID 24956427—

Reaction Steps

In a 20 mL vial 2,5-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 0.93 (t, 3 H) 1.30-1.36 (m, 2 H) 1.71-1.79 (m, 2 H) 2.47 (s, 3 H) 3.73 (s, 3 H) 3.80 (s, 3 H) 4.11 (t, 2 H) 6.59 (s, 1 H) 6.96-7.00 (m, 1 H) 7.02-7.06 (m, 1 H) 7.22 (d, 1 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-a0abf3ad74a74956b2c9f5200e6a434a
Source noteuspto-grants-2013_07