HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443814Generated: October 31, 2026
Carbon Disulfide → 5-Isothiocyanato-3-methoxymethylisoquinoline
https://huagongshe.com/reaction/443814
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 5-Amino-3-methoxymethylisoquinoline | HCID 12874852 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 5-Isothiocyanato-3-methoxymethylisoquinoline | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04261992 |
|---|
| Source dataset | uspto-grants-1981_04 |
|---|
| ORD ID | ord-9cbb245508844cb2b76b11161402d370 |
|---|
| Source note | uspto-grants-1981_04 |
|---|