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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 935생성일: 2026년 10월 24일

Dimethylformamide → cis-N-[1-[3-(4-Fluorophenoxy)propyl]-3-methoxy-4-piperidinyl]-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamide

https://huagongshe.com/ko/reaction/935

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TriethylamineHCID 8471—
반응물1-(3-Bromopropoxy)-4-fluorobenzeneHCID 260004—
반응물cis-N-(3-Methoxy-4-piperidinyl)-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamideHCID 69232145—
용매Ethyl AcetateHCID 8857—
생성물cis-N-[1-[3-(4-Fluorophenoxy)propyl]-3-methoxy-4-piperidinyl]-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamideHCID 6922949891.8%

반응 조건

온도50 °C

반응 단계

A mixture comprising 0.10 g of the cis-N-(3-methoxy-4-piperidinyl)-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamide, 0.07 g of 3-(4-fluorophenoxy)propyl bromide, 0.20 g of triethylamine and 10 ml of DMF was stirred at 50° C. for 2 hours and cooled. Ethyl acetate was poured into the resulting mixture. The obtained mixture was washed with water thrice, dried over magnesium sulfate, and freed from the solvent. The residue was purified by silica gel column chromatography (5% methanol/dichloromethane) to give 0.13 g of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723472
출처 데이터셋uspto-grants-1998_03
ORD IDord-e90e3b33efd8427982a8d67e8d113a2f
출처 메모uspto-grants-1998_03