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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 924154Generated: October 31, 2026

(3-Cyano-5-fluorophenyl)boronic acid → HCID 89907725, compound

https://huagongshe.com/reaction/924154

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Cyano-5-fluorophenyl)boronic acidHCID 23435605—
Reactant(R)-5-Bromo-N-(4-(chlorodifluoromethoxy)phenyl)-6-(3-hydroxypyrrolidin-1-yl)nicotinamideHCID 72545856—
ProductHCID 89907725HCID 89907725—

Reaction Steps

The title compound was prepared in an analogous fashion to that described in Example 290 using (R)-5-bromo-N-(4-(chlorodifluoromethoxy)phenyl)-6-(3-hydroxypyrrolidin-1-yl)nicotinamide (Stage 171.1) and 3-Cyano-5-Fluorophenylboronic acid to afford a white solid. HPLC (Condition 10) tR=6.383 min, UPLC-MS (Condition 11) m/z=503.1 [M+H]+; 1H-NMR (400 MHz, DMSO-d6) δ ppm 1.69-1.80 (m, 1H) 1.81-1.93 (m, 1H) 2.86 (d, J=10.95 Hz, 1H) 3.14-3.29 (m, 2H) 3.35-3.49 (m, 1H) 4.21 (br. s, 1H) 4.87 (d, J=3.52 Hz, 1H) 7.34 (d, J=8.60 Hz, 2H) 7.67 (d, J=9.38 Hz, 1H) 7.79 (s, 1H) 7.83-7.91 (m, J=8.99 Hz, 3H) 8.06 (d, J=1.96 Hz, 1H) 8.77 (d, J=2.35 Hz, 1H) 10.17 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278981B2
Source datasetuspto-grants-2016_03
ORD IDord-e6b803b46a4645fd862213d8b50a4156
Source noteuspto-grants-2016_03