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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518334Generated: October 25, 2026

1-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2(1H)-one → US10023592, Example 118

https://huagongshe.com/reaction/518334

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2(1H)-oneHCID 45480194—
Reactant3-Bromo-4-(2,4-difluorophenoxy)benzenesulfonamideHCID 61712700—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventBicarbonate IonHCID 769—
Solvent1,4-DioxaneHCID 31275—
ProductUS10023592, Example 118HCID 11802258318%

Reaction Steps

3-Bromo-4-(2,4-difluorophenoxyl)benzenesulfonamide (1 eq., 62 mg), the title compound of Example 98, step 1 (40 mg, 0.17 mmol), Pd(dppf)Cl2 (10 mg, 8%) in 1,4-dioxane (880 μL) and saturated bicarbonate solution (aq) (220 μL) were reacted at 105° C. for 30 min in a manner similar to Example 117. Work up and preparative HPLC, also in a similar manner, gave the title compound (12 mg, 18%) as a white solid. 1H NMR (DMSO, 400 MHz): δ3.51 (s, 3H), 6.49 (d, J=9.4, 1H), 4.15 (q, J=6.9, 2H), 6.45 (d, J=9.4 Hz, 1H), 7.20-7.23 (m, 3H), 7.64 (dd, J=2.6, 9.4 Hz, 1H), 7.72-7.74 (m, 2H), 7.89 (d, J=2.6 Hz, 1H). LCMS (M+H)+=393.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115114B2
Source datasetuspto-grants-2015_08
ORD IDord-de7f24a3c509489db19bd0928c7078f5
Source noteuspto-grants-2015_08