Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988832Generated: November 4, 2026

Ammonium Chloride → HCID 68705712, compound

https://huagongshe.com/reaction/1988832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(3-Nitropyridin-4-yl)-1,2,3,4-tetrahydroisoquinolineHCID 68705703—
ReactantHCID 178448414HCID 178448414—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68705712HCID 6870571238.7%

Reaction Conditions

Temperature-20 °C

Reaction Steps

2-(3-Nitropyridin-4-yl)-1,2,3,4-tetrahydroisoquinoline (5 g, 19.58 mmol) prepared in Preparation 1 was dissolved in anhydrous tetrahydrofuran (200 ml) under a nitrogen atmosphere. 1-Methyl-1-propenyl magnesium bromide (0.5M in tetrahydrofuran solution, 80 ml, 117.5 mmol) was added at −78° C. to the solution, which was then stirred for 5 hours at −20° C. 20 ml of 20% ammonium chloride solution was added to the reaction mixture, which was then extracted with ethyl acetate (200 ml) twice. The separated organic layer was dried on anhydrous magnesium sulfate and then concentrated under reduced pressure. The resulting residue was purified with silica gel column chromatography (ethyl acetate/methylene chloride/methanol=10/10/1, (v/v/v)) to give the titled compound as a pale yellow solid (2.1 g, 25.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642269B2
Source datasetuspto-grants-2010_01
ORD IDord-5860c3d775c546dcb6f7f7903154858a
Source noteuspto-grants-2010_01