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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792584Generated: November 4, 2026

Dimethylamine → HCID 22032295, compound

https://huagongshe.com/reaction/1792584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantHCID 22031800HCID 22031800—
CatalystHCID 178418406HCID 178418406—
SolventChloroformHCID 6212—
ProductHCID 22032295HCID 22032295—

Reaction Steps

A mixture of 296 mg {4-[4-(3-pyridin-2-ylimidazo[1,2-a]pyridin-6-yl)-1-trityl-1H-pyrazol-3-yl]phenyl}methanol (compound in Example 359), 844 mg manganese (IV) oxide and 20 mL chloroform was heated for 1 hour under reflux. The reaction solution was cooled to remove insolubles, and the filtrate was evaporated. 264 mg crude product of 4-[4-(3-pyridin-2-ylimidazo[1,2-a]pyridin-6-yl)-1-trityl-1H-pyrazol-3-yl]benzaldehyde was obtained as a pale brown amorphous. From 100 mg of this aldehyde derivative and 35 μL dimethylamine (50% aqueous solution), 81 mg of the title compound was obtained as a colorless amorphous under the same conditions as in Production Example 153.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074801B1
Source datasetuspto-grants-2006_07
ORD IDord-6f2625f410d3427fb21178384597dbb8
Source noteuspto-grants-2006_07