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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247148Generated: October 29, 2026

Calcium Sulfate → HCID 21906405, compound

https://huagongshe.com/reaction/1247148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCalcium SulfateHCID 24497—
ReactantSodium FormateHCID 2723810—
ReactantN-(5-chloropyridin-2-yl)-5-iodo-2-[(1-isopropylpiperidin-4-ylcarbonyl)amino]benzamideHCID 21906277—
CatalystTriphenylphosphineHCID 11776—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
ProductHCID 21906405HCID 2190640562%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirring solution of N-(5-chloropyridin-2-yl)-5-iodo-2-[(1-isopropylpiperidin-4-ylcarbonyl)amino]benzamide (0.51 g, 0.97 mmol) in N,N-dimethylformamide (10 mL) was added sodium formate (0.11 g, 1.6 mmol), calcium sulfate (0.39 g, 2.9 mmol), triphenylphosphine (6 mg, 0.02 mmol) and dichlorobis(triphenylphosphine)palladium(II) (15 mg, 0.02 mmol). The reaction mixture was heated to 80° C., stirred overnight, cooled to room temperature, partitioned between dichloromethane and saturated aqueous sodium bicarbonate, and the layers separated. The organic phase was filtered to remove solids, dried over magnesium sulfate, filtered, and concentrated in vacuo. The crude product was purified by RPHPLC, eluting with a gradient of 10% through 50% acetonitrile in 0.05% aqueous hydrochloric acid, to give 0.14 g (31%) of a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129245B2
Source datasetuspto-grants-2006_10
ORD IDord-20fa7d83e774490fa652418179a8e935
Source noteuspto-grants-2006_10