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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754946Generated: October 28, 2026

Nitrogen → HCID 66816324, compound

https://huagongshe.com/reaction/1754946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantSodium CarbonateHCID 10340—
Reactant4-(Dimethylcarbamoyl)phenylboronic AcidHCID 3503767—
ReactantHCID 49838533HCID 49838533—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 66816324HCID 6681632477.5%

Reaction Steps

A mixture of 8-(5-bromo-thiophene-2-sulfonyl)-2-(3-trifluoromethyl-phenyl)-1,3,8-triaza-spiro[4.5]dec-1-en-4-one (11.1 mg, 0.0212 mmol), 4-(N,N-dimethylaminocarbonyl)phenylboronic acid (8.0 mg, 0.041 mmol), Pd(PPh3)4 (3.8 mg, 0.0033 mmol) and Na2CO3 (22.0 mg, 0.208 mmol) in toluene (0.12 ml)-EtOH (0.12 ml)-H2O (0.12 ml) was stirred at 85° C. for 20 hours in a sealed test tube in an N2 atmosphere. The reaction mixture was cooled to room temperature and extracted with AcOEt. The organic layer was washed with a saturated aqueous NH4Cl solution, and then dried over MgSO4 and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (AcOEt) to give N,N-dimethyl-4-{5-[4-oxo-2-(3-trifluoromethyl-phenyl)-1,3,8-triaza-spiro[4.5]dec-1-ene-8-sulfonyl]-thiophen-2-yl}-benzamide (9.7 mg, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169254B2
Source datasetuspto-grants-2015_10
ORD IDord-4b1ff05762fe4dfe90eff7fb172e5048
Source noteuspto-grants-2015_10