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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525807Generated: October 30, 2026

Diisopropylethylamine → HCID 86290707, compound

https://huagongshe.com/reaction/525807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl piperazine-1-acetateHCID 207112—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 51040739HCID 51040739—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86290707HCID 86290707—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 7-[3-fluoro-4-({[(2-fluoro-5-methylphenyl)amino]carbonyl}amino)phenoxy]thieno[3,2-b]pyridine-2-carboxylic acid (100 mg, 0.22 mmol), HATU (91 mg, 0.24 mmol) and N,N-diisopropylethylamine (62 mg, 0.48 mmol) in anhydrous tetrahydrofuran (10 ml) was heated at 60° C. for 10 minutes, followed by addition of ethyl piperazinoacetate (57 mg, 0.33 mmol). Heating was continued at 60° C. for 30 minutes and the mixture was poured into 100 ml of water. The precipitates were filtered, washed with water and dried in vacuo to give the crude, which was purified by silica gel chromatography eluting with 3˜5% methanol in chloroform to give ethyl [4-({7-[3-fluoro-4-({[(2-fluoro-5-methylphenyl)amino]carbonyl}amino)phenoxy]thieno[3,2-b]pyridin-2-yl}carbonyl)piperazin-1-yl]acetate as white solid. Yield: 73 mg, 54%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340555B2
Source datasetuspto-grants-2016_05
ORD IDord-283aeec5fd6546b3ab97efd5f61e75f5
Source noteuspto-grants-2016_05