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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448044Generated: October 29, 2026

3-Chlorobenzoic Acid → HCID 24956057, compound

https://huagongshe.com/reaction/448044

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chlorobenzoic AcidHCID 447—
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 24956057HCID 24956057—

Reaction Steps

In a 20 mL vial 3-chlorobenzoic 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 0.92 (t, 3 H) 1.27-1.40 (m, 2 H) 1.72-1.80 (m, 2 H) 2.47-2.50 (m, 3 H) 4.27 (t, 2 H) 6.76 (s, 1 H) 7.46-7.53 (m, 1 H) 7.52-7.57 (m, 1 H) 7.94-7.99 (m, 1 H) 8.01-8.05 (m, 1 H); MS (ESI) m/z 309 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481574B2
Source datasetuspto-grants-2013_07
ORD IDord-b2d8ca5dfc1944df9739a7cdab76b003
Source noteuspto-grants-2013_07