Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11353생성일: 2026년 10월 26일
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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | tert-butyl N-(4-aminobutyl)carbamate | HCID 4351 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 2,4-Dichloro-5,6-dimethyl-3-nitropyridine | HCID 12109123 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Tert-butyl 4-[(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)amino]butylcarbamate | HCID 12109124 | 48% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07098221B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-70c165635d014dcb99ca60dfce845323 |
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| 출처 메모 | uspto-grants-2006_08 |
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