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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5691생성일: 2026년 10월 24일

Pivalic acid → 1-(3,3-diethoxypropyl)-5-(4-fluorophenyl)-2-(1-methyl-ethyl)-N,4-diphenyl-1H-pyrrole-3-carboxamide

https://huagongshe.com/ko/reaction/5691

반응식

참여 물질

역할이름HCID투입량
반응물Pivalic acidHCID 6417—
반응물1-Amino-3,3-diethoxypropaneHCID 521029—
반응물4-(4-Fluorophenyl)-2-(2-methyl-1-oxopropyl)-4-oxo-3,N-diphenylbutanamideHCID 9909872—
용매TolueneHCID 1140—
생성물1-(3,3-diethoxypropyl)-5-(4-fluorophenyl)-2-(1-methyl-ethyl)-N,4-diphenyl-1H-pyrrole-3-carboxamideHCID 1104970581.2%

반응 조건

온도22.5 °C

반응 단계

To a nitrogen purged flask equipped with a mechanical stirrer is added 130 kg (311 mol) of (±)4-fluoro-α-[2-methyl-1-oxopropyl]-γ-oxo-N,β-diphenylbenzenebutaneamide mixture of [R-(R*,R*)], [R-(R*,S*)], [S-(R*,R*)] and [S-(R*,S*)] isomers, 540 L of heptanes and 60 L of toluene, 59 kg (400 mol) of 3-amino-1,1-diethoxypropane, and 22.3 kg (218 mol) of pivalic acid. The mixture is stirred and heated to reflux, removing water with a Dean Stark trap. The mixture is refluxed 32 hours and slowly cooled to 60°-65° C., diluted with 500 L of 2-propanol-water (3:2), seeded, and cooled to 20-25° C. The product is isolated by filtration, washed with 300 L of 2-propanol, and dried in vacuo to yield 133.5 kg of 1-(3,3-diethoxypropyl)-5-(4-fluorophenyl)-2-(1-methylethyl)-N,4-diphenyl-1 H-pyrrole-3-carboxamide; mp 125.1°-127.7° C. after recrystallization from ethanol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05245047
출처 데이터셋uspto-grants-1993_09
ORD IDord-bc325b8893574d99b132a5fdc2ef0766
출처 메모uspto-grants-1993_09