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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731743Generated: November 3, 2026

3-Pyridinylboronic acid → HCID 57837458, compound

https://huagongshe.com/reaction/731743

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Pyridinylboronic acidHCID 2734378—
ReactantHCID 57837481HCID 57837481—
ReactantHCID 57837525HCID 57837525—
ProductHCID 57837458HCID 57837458—

Reaction Steps

2-Isopropyl-3-pyridin-3-yl-pyrazolo[1,5-a]pyridine was prepared from 3-iodo-2-isopropyl-pyrazolo[1,5-a]pyridine and 3-pyridineboronic acid following the method used in Step 3 of the synthesis of 3-(2-Isopropyl-pyrazolo[1,5-a]pyridin-3-yl)-phenylamine (Example 59) (240 mg, 32%). 1H-NMR (250 MHz, DMSO-d6) δ 8.69 (d, J=7.3 Hz, 1H), 8.67 (s, 1H), 8.55 (d, J=4.0 Hz 1H), 7.85 (d, J=7.8 Hz, 2H); 7.56-7.47 (m, 1H), 7.20 (t, J=8.8 Hz, 1H), 6.89 (t, J=6.8 Hz, 1H), 3.24 (sept, J=7.0 Hz, 1H), 1.28 (d, J=6.8 Hz, 6H); LC/MS 237.9 m/z (M+H+). Compound 1111.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585875B2
Source datasetuspto-grants-2009_09
ORD IDord-879612c11b15492aa04088d7a7bd614d
Source noteuspto-grants-2009_09