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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetramethoxypropane | HCID 66019 | — |
| Reactant | 5-Hydrazinylisoquinoline | HCID 13266423 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(1H-pyrazol-1-yl)isoquinoline | HCID 86711342 | 73.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853203B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-12dc6e020a92437a830fbc4049254085 |
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| Source note | uspto-grants-2014_10 |
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