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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910695Generated: November 3, 2026

Cesium carbonate → HCID 67282367, compound

https://huagongshe.com/reaction/1910695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantTriphenylphosphineHCID 11776—
Reactant2,2-Dimethyl-N-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]propanamideHCID 57416418—
ReactantHCID 67283973HCID 67283973—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 67282367HCID 6728236737.1%

Reaction Steps

3-(Biphenyl-2-ylmethyl)-5,7-dichloro-1-methyl-1H-benzo[e][1,4]diazepin-2(3H)-one (0.192 g, 0.469 mmol), N-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)pivalamide (0.214 g, 0.703 mmol, 1.2 eq), Palladium (II) acetate (0.2 eq), triphenyl phosphine (0.2 eq) and cesium carbonate (2 eq) were heated at 100° C. in DMF (3 mL) under an atmosphere of nitrogen in a sealed tube for 1.5 h. The mixture was cooled then diluted with ethyl acetate and water (2:1) then filtered through a pad of celite. The layers were separated and the organic phase was washed with brine then dried over sodium sulfate. Chromatography eluting with 1:1 ethyl acetate in hexanes gave an oil which was dissolved in a 2:1 mixture of acetonitrile and water and freeze-dried to give product as an off-white solid (0.096 g, 37% yield). 1H-NMR (300 MHz, CDCl3) δ 8.29-8.22 (m, 2H), 8.09 (s, 1H), 7.71 (dd, 1H), 7.51-7.47 (m, 2H), 7.32-7.28 (m, 2H), 7.20-7.12 (m, 8H), 3.69-3.55 (m, 2H), 3.41-3.36 (m, 1H), 3.31 (s, 3H), 1.33 (s, 9H). MS (APCI) m/z 551 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604023B2
Source datasetuspto-grants-2013_12
ORD IDord-aae44724aefe40bbb250d460784dca58
Source noteuspto-grants-2013_12