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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923997Generated: October 30, 2026

(5-Fluoropyridin-3-yl)boronic acid → HCID 118195377, compound

https://huagongshe.com/reaction/923997

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5-Fluoropyridin-3-yl)boronic acidHCID 44717403—
Reactant5-bromo-6-(ethyl(2-hydroxyethyl)amino)-N-(4-(trifluoromethoxy)phenyl)nicotinamideHCID 89906577—
ProductHCID 118195377HCID 118195377—

Reaction Steps

The title compound was prepared in an analogous fashion to that described in Example 151 using 5-bromo-6-(ethyl(2-hydroxyethyl)amino)-N-(4-(trifluoromethoxy)phenyl)nicotinamide (Stage 156.1) and (5-fluoropyridin-3-yl)boronic acid to afford a white solid. UPLC-MS (Condition 3) tR=1.09 min, m/z=465.3 [M+H]+, m/z=463.4 [M−H]−; 1H-NMR (400 MHz, DMSO-d6) δ ppm 0.90 (t, J=7.03 Hz, 3H) 3.16 (q, J=7.03 Hz, 2H) 3.35-3.42 (m, 2H) 3.49 (br. s, 2H) 4.62 (br. s, 1H) 7.36 (d, J=8.41 Hz, 2H) 7.80-7.89 (m, 2H) 7.98 (m, J=2.70, 1.82 Hz, 1H) 8.08 (d, J=2.38 Hz, 1H) 8.60 (d, J=2.76 Hz, 1H) 8.64 (t, J=1.63 Hz, 1H) 8.76 (d, J=2.38 Hz, 1H) 10.26 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278981B2
Source datasetuspto-grants-2016_03
ORD IDord-59cdb31520ff42ca8b571afa78c92d23
Source noteuspto-grants-2016_03