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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402541Generated: October 31, 2026

2,2-Diethoxyethylamine → HCID 71543003, compound

https://huagongshe.com/reaction/1402541

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-DiethoxyethylamineHCID 69524—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 51001123HCID 51001123—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 71543003HCID 71543003—

Reaction Steps

A mixture of 5-{4-[3-fluoro-4-({[(2-fluoro-5-methylphenyl)amino]carbonyl}amino)phenoxy]pyridin-2-yl}-1H-pyrrole-3-carboxylic acid (500 mg, 1.08 mmol), HATU (456 mg, 1.20 mmol) and N,N-diisopropylethylamine (278 mg, 2.16 mmol) in anhydrous DMF (10 ml) was stirred at room temperature for 10 minutes, followed by addition of aminoacetaldehyde diethyl acetal (173 mg, 1.30 mmol). The mixture was stirred for another 10 minutes and poured into 100 ml of water. The precipitates were filtered, washed with water and dried in vacuo to give N-(2,2-diethoxyethyl)-5-{4-[3-fluoro-4-({[(2-fluoro-5-methylphenyl)amino]carbonyl}amino)phenoxy]pyridin-2-yl}-1H-pyrrole-3-carboxamide as white solid. Yield: 550 mg, 88%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906944B2
Source datasetuspto-grants-2014_12
ORD IDord-cc6a7e2cbe4948f7bc3b70e69b5533d2
Source noteuspto-grants-2014_12