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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696213Generated: November 1, 2026

Triethylamine → HCID 67278437, compound

https://huagongshe.com/reaction/1696213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantHCID 67278153HCID 67278153—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67278437HCID 67278437—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 4-{[(1S,2R)-2-methylcyclohexyl]amino}-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid (3.9 g) and triethylamine (5.11 mL) in dioxane (39 mL) was added diphenylphosphoryl azide (5.0 mL) and the mixture was stirred at 120° C. for 3 hours. To the mixture were added EtOAc and water. The organic layer was separated and extracted with EtOAc. The extract was washed with saturated aqueous sodium hydrogencarbonate and brine, dried over MgSO4, filtrated and evaporated. The residue was purified by column chromatography on silica gel with EtOAc and n-hexane (1:4 to 1:2) to give 1-[(1S,2R)-2-methylcyclohexyl]-6-{[2-(trimethylsilyl)ethoxy]methyl}-3,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridin-2(1H)-one (3.33 g) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163767B2
Source datasetuspto-grants-2012_04
ORD IDord-78374331d496466c94056e15c9fa0c99
Source noteuspto-grants-2012_04