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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370249Generated: October 29, 2026

1,2,3,4-Tetrahydroisoquinoline → HCID 15285681, compound

https://huagongshe.com/reaction/370249

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,3,4-TetrahydroisoquinolineHCID 7046—
ReactantFumaric AcidHCID 444972—
ReactantN-(2,3-epoxypropyl)-4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidineHCID 15285697—
SolventEthanolHCID 702—
SolventIsopropanolHCID 3776—
ProductHCID 15285681HCID 15285681—

Reaction Steps

A mixture of N-[3-(2,3-epoxy)propyl]-4-(6-fluoro-1,2-benzisoxaz-3-yl)piperidine (3.56 g, 12.9 mmol) and 1,2,3,4-tetrahydroisoquinoline (2.06 g, 15.4 mmol) in isopropyl alcohol (150 ml) was heated at reflux for 4 hours. At the end of the reaction, the solvent was removed. The residual oil was purified by flash chromatography over a silica gel column (SiO2, 45 g, eluted with 1% CH3OH: 99% methylene chloride). The product thus purified as a light oil, weighed 4.15 g. The oil was treated with a solution of fumaric acid (1.98 gm, 17 mmol) in ethanol. The white crystals so obtained were recrystallized in a large volume of hot ethanol (~150 ml). the recrystallized crystals weighed 2.75 g, m.p. 179-181° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140345
Source datasetuspto-grants-2000_10
ORD IDord-876cbd08a5004e4f9ad7f6ac9a9a63bc
Source noteuspto-grants-2000_10