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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 441500생성일: 2026년 10월 25일

Hydrochloric Acid → N-(1-methylpyrrolidin-2-ylmethyl)-6-chloro-5-ethylamino-3-methoxypyrazine-2-carboxamide

https://huagongshe.com/reaction/441500

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물1-Methylpyrrolidine-2-methylamineHCID 117300—
반응물Methyl 5-ethylamino-6-chloro-3-methoxypyrazine-2-carboxylateHCID 21418994—
용매TolueneHCID 1140—
생성물N-(1-methylpyrrolidin-2-ylmethyl)-6-chloro-5-ethylamino-3-methoxypyrazine-2-carboxamideHCID 21419028—

반응 단계

To 30 ml. of toluene were added 3.0 g. of methyl 6-chloro-5-ethylamino-3-methoxypyrazine-2-carboxylate and 3.0 g. of 2-aminomethyl-1-methylpyrrolidine and the mixture was refluxed for 4 days. The reaction mixture was acidified with hydrochloric acid at room temperature and then extracted twice each time with 30 ml. of water. From the toluene layer, 0.9 g. of methyl 6-chloro-5-ethylamino-3-methoxypyrazine-2-carboxylate used as the starting material was recovered. The extracts were combined, basified with aqueous ammonia and extracted three times each time with 30 ml. of chloroform. The extracts were combined and evaporated to dryness. By adding 50 ml. of ether to the residue formed, 1.0 g. of crystals of N-(1-methylpyrrolidin-2-ylmethyl)-6-chloro-5-ethylamino-3-methoxypyrazine-2-carboxamide were obtained. The colorless acicular crystals obtained by recrystallizing the product from a mixture of benzene and n-hexane melted at 126°-127° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04041032
출처 데이터셋uspto-grants-1977_08
ORD IDord-554b95e2f6c3405daabfa9af200388ca
출처 메모uspto-grants-1977_08