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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400526Generated: October 30, 2026

Dimethylacetamide → HCID 46852596, compound

https://huagongshe.com/reaction/400526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylacetamideHCID 31374—
Reactant2,4-Dichloro-5-[[(2-fluorophenyl)amino]sulfonyl]benzoic acidHCID 2324377—
Reactant(8aR)-Octahydropyrrolo(1,2-a)pyrazineHCID 7004239—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Solvent2-MethyltetrahydrofuranHCID 7301—
ProductHCID 46852596HCID 46852596—

Reaction Steps

To 2,4-dichloro-5-{[(2-fluorophenyl)amino]sulfonyl}benzoic acid (800 mg, 2.197 mmol) and 2-(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)-1,1,3,3-tetramethylisouronium hexafluorophosphate(V) (919 mg, 2.416 mmol) in 2-methyltetrahydrofuran (15 mL) was added (R)-octahydropyrrolo[1,2-a]pyrazine (388 mg, 3.08 mmol). The reaction was stirred at room temperature for 45 minutes at which time N,N-dimethylacetamide (1 mL) was added. The reaction was stirred for an additional 45 minutes and N,N-dimethylacetamide (3 mL) was added. The reaction was stirred for an addition 2.5 hours, diluted with 2-methyltetrahydrofuran (15 mL), and washed with a solution of 6% sodium bicarbonate and 6% brine (2×15 mL). The aqueous layers were combined and re-extracted with 2-methyltetrahydrofuran (15 mL). The organic layer was washed with saturated brine (4×25 mL), dried over MgSO4, and concentrated. The residue was taken up in ethanol (20 mL) and reconcentrated to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741899B2
Source datasetuspto-grants-2014_06
ORD IDord-584b65f02983455c883a0d3c51251253
Source noteuspto-grants-2014_06