Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907950Generated: October 29, 2026

Acetone → HCID 86627656, compound

https://huagongshe.com/reaction/1907950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantDichloromethaneHCID 6344—
ReactantHydrazineHCID 9321—
ReactantHCID 67052268HCID 67052268—
SolventEthanolHCID 702—
ProductHCID 86627656HCID 86627656—

Reaction Steps

Anhydrous hydrazine (0.91 mL, 29 mmol) was added to a stirred suspension of N-[4-(8-{[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)oxy]methyl}-5,6-dimethyl-7H-imidazo[4,5-c]tetraazolo[1,5-a]pyridin-7-yl)butyl]-2-methylpropanamide (4.90 g, 9.71 mmol) in ethanol (100 mL). Dichloromethane (50 mL) was added. After four hours, acetone (50 mL) was added and the reaction mixture was stirred overnight. A solid was removed by filtration and washed with methanol. The filtrate was concentrated to provide a solid that was triturated with 1:1 saturated aqueous sodium bicarbonate/water. The solid was isolated by filtration, washed with water, and dissolved in chloroform (300 mL). The solution was washed with water (2×50 mL), dried over sodium sulfate, filtered, concentrated under reduced pressure, and dried under vacuum to afford N-{4-[5,6-dimethyl-8-({[(1-methylethylidene)amino]oxy}methyl)-7H-imidazo[4,5-c]tetraazolo[1,5-a]pyridin-7-yl]butyl}-2-methylpropanamide that was used in the next experiment.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598192B2
Source datasetuspto-grants-2013_12
ORD IDord-434ad99184494779b1bbf459eb9f5f68
Source noteuspto-grants-2013_12