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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525268Generated: November 1, 2026

Cesium carbonate → HCID 178420802, compound

https://huagongshe.com/reaction/525268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantHCID 5303318HCID 5303318—
ReactantHCID 178479268HCID 178479268—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 178420802HCID 178420802—

Reaction Conditions

Temperature90 °C

Reaction Steps

As shown in step 5-iii of Scheme 5, a mixture of 4-bromo-6-morpholinobenzo[c][1,2,5]oxadiazole (compound 1012, 147 mg, 0.5 mmol), (cis)-N1-(pyrimidin-2-yl)cyclohexane-1,4-diamine hydrochloride (120 mg, 0.6 mmol), (rac)-BINAP (32 mg, 0.05 mmol), Pd2(dba)3 (24 mg, 0.026 mmol), and cesium carbonate (506 mg, 1.55 mmol) in toluene (5 mL) was flushed with nitrogen gas and stirred overnight at 90° C. under an atmosphere of nitrogen. The mixture was filtered though a layer of diatomaceous earth, concentrated under reduced pressure, and purified by medium pressure silica gel chromatography (0 to 80% EtOAc/hexanes gradient) to provide (cis)-N1-(6-morpholinobenzo[c][1,2,5]oxadiazol-4-yl)-N4-(pyrimidin-2-yl)cyclohexane-1,4-diamine (compound 23) as an orange solid: 1H-NMR (300 MHz, CDCl3) δ 8.20 (d, J=4.9 Hz, 2H), 6.46 (t, J=4.8 Hz, 1H), 6.05 (d, J=1.6 Hz, 1H), 5.82 (s, 1H), 5.24 (s, 1H), 4.82 (d, J=7.0 Hz, 1H), 3.98 (s, 1H), 3.85-3.72 (m, 4H), 3.60 (s, 1H), 3.23-3.06 (m, 4H), 1.95-1.62 (m, 8H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340557B2
Source datasetuspto-grants-2016_05
ORD IDord-cdba3f0feae446e29638993007732ab0
Source noteuspto-grants-2016_05