Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 360013생성일: 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/360013
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pivalic acid | HCID 6417 | — |
| 반응물 | 1-Amino-3,3-diethoxypropane | HCID 521029 | — |
| 반응물 | 4-(4-Fluorophenyl)-2-(2-methyl-1-oxopropyl)-4-oxo-3,N-diphenylbutanamide | HCID 9909872 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 1-(3,3-diethoxypropyl)-5-(4-fluorophenyl)-2-(1-methyl-ethyl)-N,4-diphenyl-1H-pyrrole-3-carboxamide | HCID 11049705 | 81.2% |
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, 5%0 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 1o 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-lH-pyrrole-3-carboxamide; mp 125.1°-127.7° C. after recrystallization from ethanol
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05003080 |
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| 출처 데이터셋 | uspto-grants-1991_03 |
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| ORD ID | ord-8a64b544e7f141a48d4d34f61082a2d9 |
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| 출처 메모 | uspto-grants-1991_03 |
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