Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976113Generated: October 29, 2026

HCID 14115670, compound → HCID 178437163, compound

https://huagongshe.com/reaction/1976113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 14115670HCID 14115670—
ReactantHCID 178430658HCID 178430658—
ReactantHCID 178465517HCID 178465517—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 178437163HCID 178437163—

Reaction Steps

7-[N2,N3-Bis(benzyloxycarbonyl)guanidino]-8-methylquinoline. To a pale yellow solution of 500 mg of 7-amino-8-methylquinoline in 20 mL of tetrahydrofuran are added 1.18 g of ethyl N,N-bis(benzyloxy-carbonyl)pseudothiourea and 1.01 g of mercuric acetate and the mixture is stirred at room temperature for 1 hour. The suspension is diluted with ethyl acetate and the organic layer is washed with water followed by brine. The aqueous layers are extracted with ethyl acetate; the combined organic layers are dried over magnesium sulfate, filtered and rotary evaporated. The residue is purified by flash column chromatography on silica gel, eluting with 50% ethyl acetate/hexanes and recrystallization from hexanes/methylene chloride to provide 1.257 g of 7-[N2,N3-bis(benzyloxycarbonyl)guanidino]-8-ethylquinoline as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06225331B1
Source datasetuspto-grants-2001_05
ORD IDord-657acd9daa804767863a5934dd8ca44e
Source noteuspto-grants-2001_05