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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488865Generated: October 27, 2026

Diethyl Ether → (E)-3-(3-Amino-4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)-prop-2-enenitrile L-serineamide Hydrochloride

https://huagongshe.com/reaction/1488865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantChloroformHCID 6212—
Reactant(E)-3-(3-Amino-4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)-prop-2-enenitrile Fmoc-L-serineamideHCID 22877902—
SolventPiperidineHCID 8082—
Product(E)-3-(3-Amino-4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)-prop-2-enenitrile L-serineamide HydrochlorideHCID 2287791148%

Reaction Steps

(E)-3-(3-Amino-4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)-prop-2-enenitrile-Fmoc-L-serineamide (1,430 mg, 2.07 mmols) were dissolved in 5 ml of chloroform and 2 ml of piperidine. The reaction was conducted for 1 hour, and the product was then purified using a silica-gel column (eluent, mixture of ethyl acetate and dichloromethane at a ratio by volume of 1:1). The thus-purified product was concentrated to dryness under reduced pressure, and then dissolved in 10 ml of a solution of 4-M hydrochloric acid and dioxane. The resulting mixture was reacted at 70 ° C. for 1 hour. One-hundred milliliters of diethyl ether were added thereto, and the resulting precipitate was collected by filtration. The thus-obtained powder was purified through medium-pressure liquid chromatography (ODS, mixture of water and acetonitrile at a ratio by volume of from 75:25), and was heat-dissolved in a mixture of chloroform and methanol at a ratio of 5:1 to produce 460 mg (0.992 mmols) of the final product in a yield of 48%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05674906
Source datasetuspto-grants-1997_10
ORD IDord-434b2925ded348ed9898320f1c918602
Source noteuspto-grants-1997_10