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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118055Generated: October 31, 2026

Pyridine → HCID 9935206, compound

https://huagongshe.com/reaction/2118055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDimethylsulphamoyl chlorideHCID 83372—
Reactant8-Chloro-1-(3,4,5,6-tetrahydro-2h-[1,2']bipyridinyl-4-yl)-5,6-dihydro4h-2,3,5,10b-tetraaza-benzo[e]azuleneHCID 11326488—
SolventDichloromethaneHCID 6344—
ProductAmmoniaHCID 222—
ProductHCID 9935206HCID 993520668.3%

Reaction Steps

Dimethylsulphamoyl chloride (0.12 ml, 1.08 mmol) was added to a solution of the amine from example 4 (140 mg, 0.36 mmol) and pyridine (90 μl, 1.08 mmol) in dichloromethane (8 ml), and the reaction mixture was stirred at room temperature for 18 hours. TLC analysis showed that starting material remained, so additional dimethylsulphamoyl chloride (0.08 ml, 0.72 mmol) was added and the mixture was stirred for a further 24 hours. The mixture was washed with saturated aqueous sodium bicarbonate solution, dried over magnesium sulphate, and evaporated under reduced pressure. The crude product was purified by column chromatography on silica gel using dichloromethane:methanol:0.88 ammonia (95:5:0.5) as eluant, to afford the title compound as a pale yellow gum (120 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442795B2
Source datasetuspto-grants-2008_10
ORD IDord-4a12b85f83f2403d82bd047273ef19c3
Source noteuspto-grants-2008_10