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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514498Generated: October 25, 2026

(2,3-Dihydro-1-benzofuran-7-yl)methanol → 2-[5-(2,3-Dihydro-1-benzofuran-7-ylmethoxy)pyrazol-1-yl]pyridine-4-carbonitrile

https://huagongshe.com/reaction/514498

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2,3-Dihydro-1-benzofuran-7-yl)methanolHCID 2795020—
ReactantHCID 178510213HCID 178510213—
Product2-[5-(2,3-Dihydro-1-benzofuran-7-ylmethoxy)pyrazol-1-yl]pyridine-4-carbonitrileHCID 86725616—

Reaction Steps

The title compound was prepared from 2-(5-hydroxy-1H-pyrazol-1-yl)pyridine-4-carbonitrile and 2,3-dihydro-1-benzofuran-7-ylmethanol according to the procedure for the preparation of Example 39, part C. 1H NMR (400 MHz, CDCl3): δ 3.27 (2H, q, J=8.8 Hz), 4.68 (2H, q, J=8.8 Hz), 5.21 (2H, s), 5.83 (1H, d, J=2.0 Hz), 6.86 (1H, q, J=7.6 Hz), 7.17 (1H, d, J=7.6 Hz), 7.22 (1H, d, J=7.2 Hz), 7.37 (1H, dd, J=1.2 Hz, 4.8 Hz), 7.58 (1H, d, J=2.0 Hz), 8.14 (1H, s), 8.70 (1H, d, J=4.8 Hz). [M+H] Calc'd for C18H14N4O2, 319. Found, 319.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09107916B2
Source datasetuspto-grants-2015_08
ORD IDord-95e35a1be0b84abd87fc7eacd0be7865
Source noteuspto-grants-2015_08