Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441496Generated: October 26, 2026

Isopropanol → N-(2-diethylaminoethyl)-6-chloro-5-ethylamino-3-methoxypyrazine-2-carboxamide

https://huagongshe.com/reaction/441496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantN,N-DiethylethylenediamineHCID 60993—
ReactantMethyl 5-ethylamino-6-chloro-3-methoxypyrazine-2-carboxylateHCID 21418994—
SolventDiethyl EtherHCID 3283—
ProductN-(2-diethylaminoethyl)-6-chloro-5-ethylamino-3-methoxypyrazine-2-carboxamideHCID 21418988—

Reaction Steps

In 14 ml. of isopropyl alcohol were dissolved 1.4 g. of methyl 6-chloro-5-ethylamino-3-methoxypyrazine-2-carboxylate and 1.4 g. of N,N-diethylethylenediamine and the solution was refluxed for 4 days. After the reaction was over, the solvent was distilled off under reduced pressure from the reaction mixture and the residue obtained was applied to a silica gel column chromatography. The column was then developed using a mixture of ether and N-hexane of 1:1 volume ratio as an eluting solution. From the 1st fraction 0.7 g. of methyl 5-ethylamino-6-chloro-3-methoxypyrazine-2-carboxylate used as the starting material was recovered and from the 2nd fraction 0.7 g. of colorless plate crystals of N-(2-diethylaminoethyl)-6-chloro-5-ethylamino-3-methoxypyrazine-2-carboxamide a melting at 142° C. were obtained. The product obtained by recrystallizing the crystals from a mixture of benzene and n-hexane melted at 142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04041032
Source datasetuspto-grants-1977_08
ORD IDord-e6ba23b8a2444e7e99d45698f22728de
Source noteuspto-grants-1977_08