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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448069Generated: October 29, 2026

5-Bromo-2-chlorobenzoic acid → HCID 69188223, compound

https://huagongshe.com/reaction/448069

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-chlorobenzoic acidHCID 33127—
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 69188223HCID 69188223—

Reaction Steps

In a 20 mL vial 5-bromo-2-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 0.89 (t, 3 H) 1.25-1.36 (m, 2 H) 1.68-1.76 (m, 2 H) 2.51 (s, 3 H) 4.16 (t, 2 H) 6.26 (s, 1 H) 7.42-7.46 (m, 1 H) 7.58-7.63 (m, 1 H) 7.65-7.68 (m, 1 H); MS (ESI) m/z 387 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481574B2
Source datasetuspto-grants-2013_07
ORD IDord-636cde53920b4af089b30634723c9197
Source noteuspto-grants-2013_07