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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490976Generated: October 29, 2026

2,6-Pyridinedicarboxamide, N,N,N',N'-tetrakis(1-methylethyl)- → HCID 178457641, compound

https://huagongshe.com/reaction/1490976

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Pyridinedicarboxamide, N,N,N',N'-tetrakis(1-methylethyl)-HCID 343121—
ReagentBis(pinacolato)diboraneHCID 2733548—
Reagent8-([2,2'-bipyridin]-5-yl)quinolin-2(1H)-oneHCID 164681385—
CatalystBis(1,5-cyclooctadiene)dimethoxydiiridiumHCID 76001521—
CatalystPotassium tert-butoxideHCID 86639980—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178457641HCID 17845764189%

Reaction Conditions

Temperature80 °C

Reaction Steps

In an argon filled glove box, a 5.0 mL wheaton microreactor was charged with [Ir(cod)(OMe)]2 (1.98 mg, 1.5 mol%), L1 ligand (2.1 mg, 3.5 mol%), B2pin2 (50.8 mg, 1.0 equiv.), KOtBu (1.0 mg, 4.5 mol%) and dry THF (1.0 mL). The reaction mixture was stirred for 2 minutes at room temperature. To this mixture, N2,N2,N6,N6-tetraisopropylpyridine-2,6-dicarboxamide (66.7 mg, 0.2 mmol) was added. The microreactor was capped with a teflon pressure cap and placed into pre-heated aluminum block at 80 oC. The reaction mixture was stirred for 12 h. After completion (judged by GC/MS), THF was removed under reduced pressure and dried on an oil bath at 90 oC for 30 minutes, which gave the meta-borylated product 8i (81.8 mg, 89%) as off white solid.

Provenance & Evidence

DOI10.1002/anie.201809929
Source datasetBorylation dataset from Roche
ORD IDord-a87e6aee7a184527859efe9e36e2af95
Source noteBorylation dataset from Roche