Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1815003생성일: 2026년 10월 25일
tert-butyl N-(4-aminobutyl)carbamate → Tert-butyl 4-(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)butylcarbamate
https://huagongshe.com/reaction/1815003
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | tert-butyl N-(4-aminobutyl)carbamate | HCID 4351 | — |
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 2,4-Dichloro-5,6-dimethyl-3-nitropyridine | HCID 12109123 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | Tert-butyl 4-(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)butylcarbamate | HCID 21973830 | 79.8% |
반응 단계
Tert-butyl 4-aminobutylcarbamate (60 g, 339 mmol) was slowly added to a mixture of 2,4-dichloro-5,6-dimethyl-3-nitropyridine (50 g, 226 mmol), anhydrous N,N-dimethylformamide (500 mL) and triethylamine (50 mL, 339 mmol). The reaction mixture was allowed to stir overnight and then it was concentrated under reduced pressure to provide an oil. The oil was dissolved in ethyl acetate and then washed with water. The organic layer was dried over magnesium sulfate and then concentrated under reduced pressure to provide a dark oil. This material was purified by column chromatography (silica gel eluting with 40/60 ethyl acetate/hexanes) to provide 64.5 g of tert-butyl 4-(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)butylcarbamate as a bright orange oil which solidified on standing.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06878719B2 |
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| 출처 데이터셋 | uspto-grants-2005_04 |
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| ORD ID | ord-a4e528e845d94c189584dfcd74255a8e |
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| 출처 메모 | uspto-grants-2005_04 |
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