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HRID 360013作成日:2026年10月24日
Pivalic acid → 1-(3,3-diethoxypropyl)-5-(4-fluorophenyl)-2-(1-methyl-ethyl)-N,4-diphenyl-1H-pyrrole-3-carboxamide
https://huagongshe.com/ja/reaction/360013
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Pivalic acid | HCID 6417 | — |
| 反応物 | 1-Amino-3,3-diethoxypropane | HCID 521029 | — |
| 反応物 | 4-(4-Fluorophenyl)-2-(2-methyl-1-oxopropyl)-4-oxo-3,N-diphenylbutanamide | HCID 9909872 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 1-(3,3-diethoxypropyl)-5-(4-fluorophenyl)-2-(1-methyl-ethyl)-N,4-diphenyl-1H-pyrrole-3-carboxamide | HCID 11049705 | 81.2% |
反応手順
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
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05003080 |
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| 出典データセット | uspto-grants-1991_03 |
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| ORD ID | ord-8a64b544e7f141a48d4d34f61082a2d9 |
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| 出典メモ | uspto-grants-1991_03 |
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