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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869163Generated: November 2, 2026

Guanidine Hydrochloride → HCID 178479504, compound

https://huagongshe.com/reaction/1869163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidine HydrochlorideHCID 5742—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 86594800HCID 86594800—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 178479504HCID 178479504—

Reaction Conditions

Temperature25 °C

Reaction Steps

20 cm3 of methanol and 14 cm3 (7 mmol) of a 0.5M solution of sodium methoxide in methanol are added to 0.67 g (7 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). 30 cm3 of tetrahydrofuran and 0.525 g (1.4 mmol) of 3-chlorocarbonyl-1-(8-(trifluoromethyl)quinol-4-yl)-1H-indole hydrochloride, suspended in 30 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 product obtained is triturated in 20 cm3 of diisopropyl ether and filtered off, resulting in 0.14 g of 3-guanidinocarbonyl-1-(8-(trifluoromethyl)quinol-4-yl)-1H-indole hydrochloride in the form of a white powder melting at 212° 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-078bea8ce5214d7eb900d2ac87bd0643
Source noteuspto-grants-2009_12