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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055689Generated: November 1, 2026

Diisopropylethylamine → N-{2,4-Dimethyl-5-[6-(pyridin-3-yl)-1H-imidazo[1,2-b]pyrazol-1-yl]phenyl}-3-formyl-5-(penta-fluoro-lambda6-sulphanyl)benzamide

https://huagongshe.com/reaction/1055689

Reaction equation

Participants

RoleNameHCIDCharge
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—
ReactantHCID 89699939HCID 89699939—
Reactant3-Formyl-5-(pentafluoro-lambda6-sulphanyl)benzoic acidHCID 89699991—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-{2,4-Dimethyl-5-[6-(pyridin-3-yl)-1H-imidazo[1,2-b]pyrazol-1-yl]phenyl}-3-formyl-5-(penta-fluoro-lambda6-sulphanyl)benzamideHCID 86690986—

Reaction Steps

214 mg (0.659 mmol, 85% pure) of the compound from Example 36A and 301 mg (0.791 mmol) of HATU were dissolved in 2.3 ml of anhydrous DMF, and 140 μl (0.791 mmol) of N,N-diisopropylethylamine were added. After 30 min, 200 mg (0.659 mmol) of the compound of Example 11A were added. After the reaction mixture had been stirred at RT for 1.5 h, about 50 ml of water were added and the mixture was extracted three times with in each case about 50 ml of ethyl acetate. The combined organic extracts were washed with saturated sodium chloride solution, dried over anhydrous magnesium sulphate, filtered and freed from the solvent on a rotary evaporator. The crude product obtained in this manner was purified by MPLC (30 g of silica gel, mobile phase gradient cyclohexane/ethyl acetate 1:1→1:5). Evaporation of the product fractions and drying of the residue under high vacuum gave 160 mg (36% of theory, 85% pure) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394309B2
Source datasetuspto-grants-2016_07
ORD IDord-960ebd8e1d3d47cf932f444b7ac05781
Source noteuspto-grants-2016_07