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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532890Generated: October 30, 2026

Tetramethoxypropane → 5-(1H-pyrazol-1-yl)isoquinoline

https://huagongshe.com/reaction/532890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetramethoxypropaneHCID 66019—
Reactant5-HydrazinylisoquinolineHCID 13266423—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Product5-(1H-pyrazol-1-yl)isoquinolineHCID 8671134273.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

A suspension of 5-hydrazinylisoquinoline (22.0 g, 112 mmol) in EtOH (300 mL) was treated with 1,1,3,3-tetramethoxypropane (27.7 g, 169 mmol) and the mixture was heated to 100° C. for 10 h. The reaction mixture was then concentrated in vacuo and the residue obtained taken up in DCM (500 mL) and washed with a saturated aqueous solution of NaHCO3 gas formation. The aqueous layer was extracted twice with DCM and the combined org. layers were then dried over Na2SO4, filtered and concentrated in vacuo. The crude product was purified by flash chromatography (SiO2, DCM/MeOH 95:5 to DCM/MeOH 9:1) to give the title compound (16.1 g). UPLC-MS: MS 196.1 (M+H+); UPLC rt 0.62 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853203B2
Source datasetuspto-grants-2014_10
ORD IDord-12dc6e020a92437a830fbc4049254085
Source noteuspto-grants-2014_10