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HRID 11353作成日:2026年10月27日
tert-butyl N-(4-aminobutyl)carbamate → Tert-butyl 4-[(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)amino]butylcarbamate
https://huagongshe.com/reaction/11353
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 | Triethylamine | HCID 8471 | — |
| 反応物 | 2,4-Dichloro-5,6-dimethyl-3-nitropyridine | HCID 12109123 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Tert-butyl 4-[(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)amino]butylcarbamate | HCID 12109124 | 48% |
反応手順
A solution of tert-butyl 4-aminobutylcarbamate (8.52 g, 45.24 mmol) in N,N-dimethylformamide was added to a solution of 2,4-dichloro-5,6-dimethyl-3-nitropyridine (10.00 g, 45.24 mmol) and triethylamine (12.6 mL, 90.5 mmol) in N,N-dimethylformamide (320 mL). The reaction mixture was stirred overnight and then concentrated under reduced pressure. The residue was partitioned between water and ethyl acetate. The layers were separated and the aqueous layer was extracted with ethyl acetate. The organics were combined, washed with brine and then concentrated under reduced pressure to provide a brown oily residue. This material was purified by flash chromatography (400 mL silica gel, eluting initially with 10% ethyl acetate in hexane and then increasing the gradient to 15% and then to 25%) to provide 8.1 g of tert-butyl 4-[(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)amino]butylcarbamate as a yellow solid.
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-70c165635d014dcb99ca60dfce845323 |
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| 出典メモ | uspto-grants-2006_08 |
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