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HRID 66009作成日:2026年10月25日

4-Chlorobenzylpiperazine → 2-(4'-p-Chlorobenzyl-piperazino)-5-oxo-6-carbethoxy-8-ethyl-5,8-dihydro-pyrido(2,3-d)pyrimidine

https://huagongshe.com/reaction/66009

反応式

関与物質

役割名称HCID仕込み量
反応物4-ChlorobenzylpiperazineHCID 134826—
反応物2-Chloro-5-oxo-6-carbethoxy-8-ethyl-5,8-dihydropyrido(2,3-d)pyrimidineHCID 12266805—
生成物2-(4'-p-Chlorobenzyl-piperazino)-5-oxo-6-carbethoxy-8-ethyl-5,8-dihydro-pyrido(2,3-d)pyrimidineHCID 1226680974%

反応手順

Condensation of 1-p-chlorobenzyl-piperazine with 2-chloro-5-oxo-6-carbethoxy-8-ethyl-5,8-dihydro-pyrido(2,3-d)pyrimidine, as described in Example VII, gives, in a yield of 74%, 2-(4'-p-chlorobenzyl-piperazino)-5-oxo-6-carbethoxy-8-ethyl-5,8-dihydro-pyrido(2,3-d)pyrimidine; melting point 150° C., after recrystallisation from ethyl acetate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04129737
出典データセットuspto-grants-1978_12
ORD IDord-52353e447c8043f5952fcb5206d578ee
出典メモuspto-grants-1978_12