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HRID 11350作成日:2026年10月26日
tert-butyl N-(4-aminobutyl)carbamate → Tert-butyl 4-[(2-chloro-6-methyl-3-nitropyridin-4-yl)amino]butylcarbamate
https://huagongshe.com/reaction/11350
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | tert-butyl N-(4-aminobutyl)carbamate | HCID 4351 | — |
| 反応物 | 2,4-Dichloro-6-methyl-3-nitropyridine | HCID 2784819 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Tert-butyl 4-[(2-chloro-6-methyl-3-nitropyridin-4-yl)amino]butylcarbamate | HCID 12109135 | 98.5% |
反応手順
A solution of tert-butyl 4-aminobutylcarbamate (32.12 g, 170.6 mmol) in N,N-dimethylformamide (200 mL) was added over a period of 90 minutes to a solution of 2,4-dichloro-6-methyl-3-nitropyridine (35.09 g, 169.5 mmol) in N,N-dimethylformamide (500 mL). The reaction mixture was stirred at ambient temperature overnight. The solvent was removed by vacuum distillation using a 24/40 short path distillation head and warm water. The residue was dissolved in ethyl acetate (700 mL), washed with water (3×100 mL), dried over magnesium sulfate and then concentrated under reduced pressure. The crude product was purified by column chromatography (50×450 mm silica gel eluting with 1:1 hexane:ethyl acetate) to provide 59.90 g of tert-butyl 4-[(2-chloro-6-methyl-3-nitropyridin-4-yl)amino]butylcarbamate.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07098221B2 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-fded4986a54d42f184599c02d1ee8017 |
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| 出典メモ | uspto-grants-2006_08 |
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