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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 484132생성일: 2026년 10월 24일

1-(2-Methoxyphenyl)piperazine → 3-[4-[1-(2-Methoxyphenyl)-4-piperazinyl]butyl]-2-Methyl-4-thiazolidinone

https://huagongshe.com/ko/reaction/484132

반응식

참여 물질

역할이름HCID투입량
반응물1-(2-Methoxyphenyl)piperazineHCID 1346—
반응물Sodium IodideHCID 5238—
반응물Potassium CarbonateHCID 11430—
반응물3-(4-Bromobutyl)-2-methyl-4-thiazolidinoneHCID 10490993—
용매AcetonitrileHCID 6342—
생성물3-[4-[1-(2-Methoxyphenyl)-4-piperazinyl]butyl]-2-Methyl-4-thiazolidinoneHCID 15662325—

반응 단계

A suspension of 2-methyl-3-(4-bromobutyl)-4-thiazolidinone (3.0 g), 1-(2-methoxyphenyl)piperazine (2.3 g), anhydrous K2CO3 (3.5 g) and NaI (200 mg) in 100 ml of anhydrous CH3CN was heated to 80° under N2. After 4 hours no starting material remained as judged by TLC. The mixture was cooled to room temperature, filtered and concentrated in vauco. The residue was chromatographed on silica, using EtOAc as the eluent. This provided 2.18 g of product as a clear oil which solidified in vacuo (0.1 mmHg) overnight.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05229388
출처 데이터셋uspto-grants-1993_07
ORD IDord-2c0882ffcaed4502961d6feb71a6bfa4
출처 메모uspto-grants-1993_07