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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521867Generated: October 30, 2026

Dimethylamine → HCID 52950867, compound

https://huagongshe.com/reaction/1521867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 52950783HCID 52950783—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 52950867HCID 52950867—

Reaction Conditions

Temperature90 °C

Reaction Steps

7-bromo-3-(morpholin-4-ylcarbonyl)-1-phenyl-1,4-dihydrothiochromeno[4,3-c]pyrazole 5,5-dioxide (100 mg, 0.20 mmol, 1 eq.), NaOtBu (280 mg, 0.29 mmol, 1.4 eq.) are taken in degassed toluene in a sealed tube. Tris(dibenylidene acetone)dipalladium(0) (5 mg, 0.005 mmol, 0.025 eq.), 2-ditertiary butyl phosphino-2′,4′,6′-triisopropyl biphenyl (3.5 mg, 0.008 mmol, 0.04 eq.) are then added followed by dimethylamine in THF (3 mL, 2 M) and the reaction mixture is heated at 90° C. for 16 h. After this time, reaction mixture is filtered through a celite pad, evaporated and purified by silica gel flash chromatography to afford the title compound as a pale brown solid. 1H NMR (DMSO-d6, 400 MHz): δ 7.61-7.59 (m, 3H), 7.51-7.49 (m, 2H), 7.10 (s, 1H), 6.81-6.79 (dd, J=2.6, 9.0 Hz, 1H), 6.61-6.59 (d, J=9.0 Hz, 1H), 4.76 (s, 2H), 3.96 (m, 2H), 3.65 (m, 4H), 3.59 (m, 2H), 2.97 (s, 6H). MS (ESI+): 453.0. HPLC (max plot) 91.39%; Rt 4.20 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073940B2
Source datasetuspto-grants-2015_07
ORD IDord-99bef32e76054f0b9fd881d41d423179
Source noteuspto-grants-2015_07