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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448068Generated: October 25, 2026

Diisopropylethylamine → HCID 69187933, compound

https://huagongshe.com/reaction/448068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloro-5-(trifluoromethyl)benzoic acidHCID 688182—
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 69187933HCID 69187933—

Reaction Steps

In a 20 mL vial 2-chloro-5-(trifluoromethyl)benzoic 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) 1.26-1.36 (m, 2 H) 1.69-1.76 (m, 2 H) 2.50 (s, 3 H) 4.17 (t, 2 H) 6.29 (s, 1 H) 7.69-7.76 (m, 1 H) 7.77-7.82 (m, 2 H); MS (ESI) m/z 377 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481574B2
Source datasetuspto-grants-2013_07
ORD IDord-363f74359d1c4b3dbefc9d2a9c10b848
Source noteuspto-grants-2013_07