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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630642Generated: October 31, 2026

Sodium hydride → HCID 68283587, compound

https://huagongshe.com/reaction/1630642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantHCID 68283073HCID 68283073—
Reactant2-(6-Methylpyridin-3-yl)ethyl 4-methylbenzenesulfonateHCID 86658151—
SolventDimethylformamideHCID 6228—
ProductHCID 68283587HCID 68283587—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 9-bromo-6-chloro-2,3,4,5-tetrahydro-2-methyl-1H-pyrido[4,3-b]indole (500 mg, 1.67 mmol) in DMF (5 mL), sodium hydride (200 mg, 5.0 mmol) was added. After stirring at 60° C. for 30 min., 2-(6-methylpyridin-3-yl)ethyl 4-methylbenzenesulfonate (1.2 g, 4.2 mmol) was added to the reaction mixture and stirred at the same temperature for 1 h. The progress of reaction was monitored by TLC and LCMS. The reaction mixture was quenched with water and extracted with EtOAc. The organic layer was washed with water, dried over anhydrous sodium sulfate and concentrated to obtain the crude product, which was purified by reverse phase HPLC to obtain the 9-bromo-6-chloro-2,3,4,5-tetrahydro-2-methyl-5-(2-(6-methylpyridin-3-yl)ethyl)-1H-pyrido[4,3-b]indole. 1H NMR (CD3OD, TFA salt) δ (ppm): 8.39 (s, 1H), 8.12 (d, 1H), 7.66 (d, 1H), 7.26 (d, 1H), 7.1 (d, 1H),4.67 (m, 4H), 3.7 (m, 2H), 3.27 (t, 2H), 3.18 (m, 2H), 3.15 (s, 3H), 2.69 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791132B2
Source datasetuspto-grants-2014_07
ORD IDord-fd125e72fd284a5a98e5668ecdce87af
Source noteuspto-grants-2014_07