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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869159Generated: October 31, 2026

Guanidine Hydrochloride → HCID 178479503, compound

https://huagongshe.com/reaction/1869159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidine HydrochlorideHCID 5742—
ReactantDichloromethaneHCID 6344—
ReactantSodium MethoxideHCID 10942334—
Reactant3-chlorocarbonyl-1-(7-(trifluoromethyl)quinol-4-yl)-1H-indole hydrochlorideHCID 86594798—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178479503HCID 178479503—

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 concentrated to dryness under reduced pressure (2.7 kPa). 40 cm3 of tetrahydrofuran, 40 cm3 of dichloromethane and 0.525 g (1.4 mmol) of 3-chlorocarbonyl-1-(7-(trifluoromethyl)quinol-4-yl)-1H-indole hydrochloride, suspended in 20 cm3 of tetrahydrofuran, 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 isopropyl ether and filtered off, resulting in 0.1 g of 3-guanidinocarbonyl-1-(7-(trifluoromethyl)quinol-4-yl)-1H-indole hydrochloride in the form of a white powder melting at 238° 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-b6f7d41c76da4690869a3ec8175aa955
Source noteuspto-grants-2009_12