Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591359Generated: November 1, 2026

Triethylamine → HCID 71657549, compound

https://huagongshe.com/reaction/591359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant6-Fluoro-1-(piperidin-4-yl)indolineHCID 22038384—
Reactant4-Oxo-4,5,6,7-tetrahydropyrazolo[1,5-a] pyrazine-2-carboxylic acidHCID 55264578—
SolventTetrahydrofuranHCID 8028—
ProductHCID 71657549HCID 71657549—

Reaction Steps

To a suspension of 4,5,6,7-tetrahydro-4-oxo-pyrazolo[1,5-a]pyrazine-2-carboxylic acid (181 mg, 1.0 mmol) in THF (15 mL) was added diphenylphosphoryl azide (0.25 mL, 1.0 mmol) and Et3N (0.28 mL. 2.0 mmol). The resulting mixture was heated to reflux for 6 h and cooled to room temperature. Then 6-fluoro-1-(piperidin-4-yl)indoline (88 mg, 0.4 mmol) and Et3N (0.14 mL, 1.0 mmol) were added sequentially. The resulting mixture was stirred at room temperature for 24 h and concentrated. The resulting residue was purified by chromatography using EtOAc, then 2-5% MeOH/EtOAc as the eluent to yield 4-(6-fluoroindolin-1-yl)-N-(4-oxo-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazin-2-yl)piperidine-1-carboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238658B2
Source datasetuspto-grants-2016_01
ORD IDord-ca856f801a4e40709bd111546ae06473
Source noteuspto-grants-2016_01