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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519051Generated: November 2, 2026

Potassium Carbonate → HCID 86727416, compound

https://huagongshe.com/reaction/519051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTrimethylboroxineHCID 574072—
ReactantHCID 86727379HCID 86727379—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86727416HCID 8672741656.7%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (0.0598 g, 0.073 mmol), 6-(1-benzhydryl-3-methyl-azetidin-3-ylamino)-7-bromo-4-methyl-2,10-dihydro-9-oxa-1,2,4a-triaza-phenanthren-3-one (Example #79, Step B, 0.20 g, 0.366 mmol), K2CO3 (0.152 g, 1.098 mmol), 2,4,6-trimethyl-1,3,5,2,4,6-trioxatriborinane (0.138 g, 1.098 mmol) in water (1 mL) and dioxane (6 mL) was stirred at 120° C. overnight. The reaction mixture was cooled to ambient temperature and the solvent was removed in vacuo. The residue was purified by preparative HPLC (Table 3, Method 13) to give 6-(1-benzhydryl-3-methyl-azetidin-3-ylamino)-4,7-dimethyl-2,10-dihydro-9-oxa-1,2,4a-triaza-phenanthren-3-one (0.10 g, 56%). LC/MS (Table 1, Method 2) Rt=0.959 min; MS m/z: 482 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115151B2
Source datasetuspto-grants-2015_08
ORD IDord-a382b23926bf4d648bc96e0cfec10100
Source noteuspto-grants-2015_08