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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443814Generated: October 31, 2026

Carbon Disulfide → 5-Isothiocyanato-3-methoxymethylisoquinoline

https://huagongshe.com/reaction/443814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
ReactantTriethylamineHCID 8471—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant5-Amino-3-methoxymethylisoquinolineHCID 12874852—
SolventPyridineHCID 1049—
Product5-Isothiocyanato-3-methoxymethylisoquinolineHCID 12874854—

Reaction Steps

A solution of 5-amino-3-methoxymethylisoquinoline (22.9 g) in pyridine (80 cc) is added dropwise, whilst stirring and at a temperature of about -10° C., to a solution of triethylamine (17 cc) and carbon disulphide (55 cc) in pyridine (80 cc). After 4 hours at -10° C., a solution of dicyclohexylcarbodiimide (25.2 g) in pyridine (80 cc) is added dropwise. Stirring is maintained for 3 hours at a temperature which changes from -10° to 20° C., and then for 20 hours at a temperature of about 20° C. The mixture is evaporated to dryness at 60° C. under reduced pressure (20 mm Hg), the residue is taken up in methylene chloride (800 cc), and insoluble material is removed by filtration and the filtrate is evaporated to dryness at 40° C. under reduced pressure (40 mm Hg). The residue is taken up in diisopropyl ether (1 liter; an insoluble material is removed by filtration and the filtrate is evaporated to dryness at 40° C. under reduced pressure (20 mm Hg). 5-Isothiocyanato-3-methoxymethylisoquinoline (18.5 g), m.p. 88° C., is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04261992
Source datasetuspto-grants-1981_04
ORD IDord-9cbb245508844cb2b76b11161402d370
Source noteuspto-grants-1981_04