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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1768947생성일: 2026년 10월 27일

2-Naphthoxyacetic acid → 1-[2-(2-Naphthyloxy)acetyl]-4-[2,6-di(1-pyrrolidinyl)-4-pyrimidinyl]homopiperazine

https://huagongshe.com/reaction/1768947

반응식

참여 물질

역할이름HCID투입량
반응물2-Naphthoxyacetic acidHCID 8422—
반응물1-[2,6-Di(1-pyrrolidinyl)-4-pyrimidinyl]homopiperazineHCID 18946301—
용매TetrahydrofuranHCID 8028—
생성물1-[2-(2-Naphthyloxy)acetyl]-4-[2,6-di(1-pyrrolidinyl)-4-pyrimidinyl]homopiperazineHCID 1894628628%

반응 단계

To a solution of 2-(2-naphthyloxy)acetic acid (1.1 g, 5.0 mmol) in anhydrous tetrahydrofuran (25 ml) carbonyl-diimidazole (0.80 g, 5.0 mmol) was added in portions, under stirring at room temperature. After 15 minutes a solution of 1-[2,6-di(1-pyrrolidinyl)-4-pyrimidinyl]homopiperazine (1.58 g, 5.0 mmol) in anhydrous tetrahydrofuran (15 ml) was added dropwise. The mixture was stirred at room temperature for 8 hours and the solvent was distilled off under reduced pressure. The residue was dissolved in methylene chloride, the solution was washed three times with water, dried over MgSO4 and concentrated. The obtained crude product was chromatographed over a silica gel column eluting with a 1:2 mixture of benzene and ethyl acetate to afford 0.7 g of the title compound, yield: 28%, mp. 103°-110° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05380724
출처 데이터셋uspto-grants-1995_01
ORD IDord-d6156057814448ad884c7ca6105d4e1e
출처 메모uspto-grants-1995_01