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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541849Generated: October 29, 2026

Triethylamine → HCID 178478262, compound

https://huagongshe.com/reaction/541849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCesium carbonateHCID 10796—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
ReactantN-{3-[(Z)-2-(4-Aminopyridin-2-yl)vinyl]phenyl}-2,5-dichloropyrimidin-4-amine DihydrochlorideHCID 86636271—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178478262HCID 17847826235%

Reaction Steps

To a mixture of N-{3-[(Z)-2-(4-aminopyridin-2-yl)vinyl]phenyl}-2,5-dichloropyrimidin-4-amine dihydrochloride (34.6 mg, 0.08 mmol) and triethylamine (0.034 mL, 0.24 mmol) in dry 1,4-dioxane (0.70 mL) was added (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (2.8 mg, 0.0048 mmol), palladium acetate (0.7 mg, 0.003 mmol) and cesium carbonate (52.3 mg, 0.16 mmol). The mixture was degassed by bubbling N2 through the solution. The sealed tube was then microwaved at 150° C. for 30 min. The reaction mixture was diluted with THF/MeOH, filtered and concentrated to give the residue, which was then triturated with MeOH/EtOAc/THF to provide the desired product as a light yellow powder (9 mg, 35%). LCMS for C17H13ClN5 (M+H)+: m/z=322.0. 1H NMR (300 MHz, DMSO-d6): δ 9.81 (s, 1H), 9.33 (s, 1H), 9.15 (s, 1H), 8.49 (s, 1H), 8.26 (m, 1H), 8.19 (s, 1H), 7.33 (m, 1H), 7.24 (m, 1H), 7.08 (d, J=5.7 Hz, 1H), 6.93 (dd, J=5.7, 2.1 Hz, 1H), 6.83 (m, 1H), 6.58 (d, J=13.5 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871753B2
Source datasetuspto-grants-2014_10
ORD IDord-2be50dd881c74e9693c1ea7436fd77ab
Source noteuspto-grants-2014_10