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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351680Generated: October 30, 2026

Potassium Carbonate → N-Benzyl-N-(3,4-dimethoxy-phenyl)-4-(1,4-dioxa-8-aza-spiro[4.5]dec-8-yl)-benzenesulfonamide

https://huagongshe.com/reaction/351680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-Dioxa-8-azaspiro(4.5)decaneHCID 67435—
ReactantN-Benzyl-N-(3,4-dimethoxy-phenyl)-4-fluoro-benzenesulfonamideHCID 12051199—
Solvent2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
ProductN-Benzyl-N-(3,4-dimethoxy-phenyl)-4-(1,4-dioxa-8-aza-spiro[4.5]dec-8-yl)-benzenesulfonamideHCID 12051786—

Reaction Conditions

Temperature70 °C

Reaction Steps

1,4-Dioxa-8-azaspiro[4.5]decane (0.14 ml, 0.95 mM) was added to a solution of N-Benzyl-N-(3,4-dimethoxy-phenyl)-4-fluoro-benzenesulfonamide(0.19 g, 0.47 mM) and potassium carbonate (0.66 g, 4.82 mM)in anhyrous 1,3-dimethyl-3,4,5,6-tetrahydro-2 (1H)-pyrimidinone(5 ml). The reaction was stirred at 70° C. for two days. The reaction was quenched with water(50 ml). The precipitate was washed with water and dried under reduced pressure to afford 0.15 g of the desired product as a tan solid. H1 NMR(CDCl3) δ 1.81 (t, 4H, J=5.67 Hz), 3.50(t, 4H, J=5.97 Hz), 3.65(s, 3H), 3.81 (s, 3H), 4.01 (s, 4H), 4.66(s, 2H), 6.43(d, 1H, J=2.34 Hz), 6.53(m, 1H), 6.66(d, 1H, J=8.58 Hz), 6.90 (d, 1H, J=9.03 Hz), 7.19(m, 6H), 7.53(d, 2H, J=9.00 Hz). MS(ES) m/z 525.0; (MH+); HRMS for C28H32SN2O6: 525.2049.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743787B2
Source datasetuspto-grants-2004_06
ORD IDord-689a421a2d4a4e41bcce3a897250442c
Source noteuspto-grants-2004_06