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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821184Generated: October 31, 2026

Triethylamine → 2-[3-(4-{[(phenylamino)carbonyl]amino}phenyl)-4-(1H-pyrrolo[2,3-b]pyridin-4-yl)-1H-pyrazol-1-yl]acetamide

https://huagongshe.com/reaction/1821184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantAmmonium HydroxideHCID 14923—
Reactant[3-(4-{[(phenylamino)carbonyl]amino}phenyl)-4-(1H-pyrrolo[2,3-b]pyridin-4-yl)-1H-pyrazol-1-yl]acetic acidHCID 68996013—
SolventTetrahydrofuranHCID 8028—
Product2-[3-(4-{[(phenylamino)carbonyl]amino}phenyl)-4-(1H-pyrrolo[2,3-b]pyridin-4-yl)-1H-pyrazol-1-yl]acetamideHCID 4688867613%

Reaction Steps

To a cooled (0° C.) solution of [3-(4-{[(phenylamino)carbonyl]amino}phenyl)-4-(1H-pyrrolo[2,3-b]pyridin-4-yl)-1H-pyrazol-1-yl]acetic acid (0.166 mmol) in anhydrous tetrahydrofuran (3.3 mL) was added triethylamine (0.25 mmol) and ethylchloroformate (0.18 mmol). After 30 minutes at 0° C., ammonium hydroxide (50 uL) was added and the reaction stirred at room temperature for 1 h. Concentration in vacuo followed by Gilson reverse phase HPLC furnished the title compound as a white solid (13%). ESMS [M+H]+: 452.4

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605266B2
Source datasetuspto-grants-2009_10
ORD IDord-61e19adcfaec4959aceeee5826ca44f5
Source noteuspto-grants-2009_10