戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 406209作成日:2026年10月26日

Methyl 3-butenoate → (E)-Methyl 7-(2,3-diphenyl-7,8-dihydropyrido[3,2-b]pyrazin-5(6H)-yl)hept-3-enoate

https://huagongshe.com/reaction/406209

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 3-butenoateHCID 77314—
反応物5-(Pent-4-enyl)-2,3-diphenyl-5,6,7,8-tetrahydropyrido[3,2-b]pyrazineHCID 66666348—
触媒HCID 178425456HCID 178425456—
溶媒DichloromethaneHCID 6344—
生成物(E)-Methyl 7-(2,3-diphenyl-7,8-dihydropyrido[3,2-b]pyrazin-5(6H)-yl)hept-3-enoateHCID 66665849—

反応手順

To a solution of 5-(pent-4-enyl)-2,3-diphenyl-5,6,7,8-tetrahydropyrido[3,2-b]pyrazine (step 1) (200 mg, 0.563 mmol) and methyl but-3-enoate (225 mg, 2.251 mmol) in DCM (300 ml) was added Grubbs Catalyst second generation (5 mol %, 23.88 mg, 0.028 mmol). The reaction was stirred at RT under an atmosphere of nitrogen overnight. An additional portion of Grubbs Catalyst second generation (5 mol %, 23.88 mg, 0.028 mmol) was added and stirring continued for 2.5 h. The solvent was removed in vacuo and the resulting crude was purified by chromatography on silica eluting with EtOAc/iso-hexane to afford the title compound;

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754085B2
出典データセットuspto-grants-2014_06
ORD IDord-cb671b216bce4c3a9ff3acd542238359
出典メモuspto-grants-2014_06