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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262107Generated: October 30, 2026

3-Methylisoquinolin-5-amine → HCID 22807720, compound

https://huagongshe.com/reaction/262107

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methylisoquinolin-5-amineHCID 12212055—
Reactant(S)-3-Methylthio-1,5,10,10a-tetrahydrothiazolo[3,4-b]isoquinolinium iodideHCID 12874874—
SolventPyridineHCID 1049—
ProductHCID 22807720HCID 2280772084.6%

Reaction Steps

(S)-3-Methylthio-1,5,10,10a-tetrahydrothiazolo-[3,4-b]isoquinolinium iodide (36.3 g) is added to a solution of 5-amino-3-methylisoquinoline (15.9 g) in pyridine (200 cc). The suspension obtained gradually goes into solution. After 24 hours at a temperature of about 20° C., the mixture is concentrated to dryness under reduced pressure (25 mm Hg) at 50° C. The residue is dissolved in a mixture of methylene chloride (600 cc) and N aqueous sodium hydroxide solution (400 cc). The organic phase is decanted, washed with water (200 cc), dried over magnesium sulphate, filtered and the filtrate is then concentrated to dryness under reduced pressure (40 mm Hg) at 40° C. The residue obtained is recrystallised from acetonitrile (500 cc). (S)-3-[(3-Methylisoquinol-5-yl)imino]-1,5,10,10a-tetrahydrothiazolo-[3,4-b]isoquinoline (29.2 g), which melts at 181° C., is thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04153698
Source datasetuspto-grants-1979_05
ORD IDord-2cd115a9a5ec4420b55be3509b1b83c7
Source noteuspto-grants-1979_05