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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869155Generated: October 30, 2026

Guanidine Hydrochloride → HCID 178479502, compound

https://huagongshe.com/reaction/1869155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidine HydrochlorideHCID 5742—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium MethoxideHCID 10942334—
Reactant3-chlorocarbonyl-1-(6-(trifluoromethyl)quinol-4-yl)-1H-indole hydrochlorideHCID 86594796—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 178479502HCID 178479502—

Reaction Conditions

Temperature25 °C

Reaction Steps

20 cm3 of methanol and 20 cm3 (10 mmol) of a 0.5M solution of sodium methoxide in methanol are added to 0.955 g (10 mmol) of guanidine hydrochloride under an argon atmosphere. After stirring at a temperature in the region of 25° C. for 1 hour, the reaction mixture is concentrated to dryness under reduced pressure (2.7 kPa) and the residue is three times successively dissolved in 20 cm3 of dichloromethane and evaporated to dryness under reduced pressure (2.7 kPa). 40 cm3 of tetrahydrofuran and 0.75 g (2 mmol) of 3-chlorocarbonyl-1-(6-(trifluoromethyl)quinol-4-yl)-1H-indole hydrochloride, suspended in 20 cm3 of dichloromethane, are subsequently added thereto under an argon atmosphere. After stirring at a temperature in the region of 20° C. for 16 hours, the reaction mixture is concentrated to give a solid which is purified by flash chromatography [eluent: ethyl acetate/methanol (9/1 and then 8/2 by volume)]. After concentrating the fractions to dryness under reduced pressure (2.7 kPa), the solid obtained is triturated in 20 cm3 of isopropyl ether and filtered off, resulting in 0.54 g of 3-guanidinocarbonyl-1-(6-(trifluoromethyl)quinol-4-yl)-1H-indole hydrochloride in the form of a white powder melting at 260° C. Mass spectrum (EI): m/e 397 (M+•), m/e 339 (base peak).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07638521B2
Source datasetuspto-grants-2009_12
ORD IDord-e8046a7648934e4982679387ece12805
Source noteuspto-grants-2009_12