Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246948Generated: October 30, 2026

Water → HCID 53855063, compound

https://huagongshe.com/reaction/246948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPiperazineHCID 4837—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 86741856HCID 86741856—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
ProductHCID 53855063HCID 5385506370.4%

Reaction Steps

In 2 ml of methylene chloride was dissolved 130 mg of anhydrous piperazine, and 200 mg of ethyl 2-[2-(2,4-difluorophenylamino)-5-fluoro-6-(2,4,6-trimethylbenzenesulfonyloxy)nicotinyl]acetate was added thereto with ice-cooling, after which the resulting mixture was subjected to reaction at the same temperature for 40 minutes. Subsequently, the reaction mixture was added to a mixture of 10 ml of ethyl acetate and 10 ml of water, and the organic layer was separated, washed successively with 2 ml of saturated aqueous sodium hydrogencarbonate solution and 2 ml of saturated aqueous sodium chloride solution, and then dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure, and to the crystalline material thus obtained was added 1 ml of n-hexane, after which crystals were collected by filtration to obtain 110 mg (yield 69.9%) of ethyl 2-[2-(2,4-difluorophenylamino)-5-fluoro-6-(1-piperazinyl)nicotinyl]acetate. The physical properties of this compound were identical with those of the compound obtained in Example 30.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04704459
Source datasetuspto-grants-1987_11
ORD IDord-21b83d9590bb4721ac3bd1c2f939c81f
Source noteuspto-grants-1987_11