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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408663Generated: October 30, 2026

4-Bromobenzenesulfonamide → HCID 68283979, compound

https://huagongshe.com/reaction/2408663

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobenzenesulfonamideHCID 69696—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant5-Ethynyl-2,8-dimethyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indoleHCID 59455000—
SolventWaterHCID 962—
ProductHCID 68283979HCID 68283979—

Reaction Steps

A mixture of 4-bromobenzenesulfonamide (200 mg, 0.84 mmol), 5-ethynyl-2,8-dimethyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (391 mg, 1.0 mmol), TBAF.3H2O (793 mg, 2.5 mmol) and dichloro bis(triphenyl phosphine) palladium (II) (29 mg, 0.042 mmol) was stirred at 85° C. for 10 min. The reaction mixture was poured into water and extracted with EtOAc (3×50 mL). The organic layer was washed with water (3×100 mL), dried over anhydrous sodium sulfate and concentrated to afford crude material, which was purified by column chromatography using neutral alumina and 5% MeOH-DCM, followed by reverse phase HPLC to yield 4-(2,8-dimethyl-1,2,3,4-tetrahydro-pyrido[4,3-b]indol-5-ylethynyl)-benzenesulfonamide. 1H NMR (CD3OD, HCl salt) δ (ppm): 7.92 (d, 2H), 7.7 (d, 2H), 7.58 (d, 1H), 7.38 (s, 1H), 7.23 (d, 1H), 4.7 (d, 1H), 4.4 (d, 1H), 3.96 (m, 1H), 3.63 (m, 1H), 3.37 (m, 2H), 3.18 (s, 3H), 2.42 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815843B2
Source datasetuspto-grants-2014_08
ORD IDord-6926ef209e7f4121a0611b73b32bfb19
Source noteuspto-grants-2014_08