Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11350생성일: 2026년 10월 26일
tert-butyl N-(4-aminobutyl)carbamate → Tert-butyl 4-[(2-chloro-6-methyl-3-nitropyridin-4-yl)amino]butylcarbamate
https://huagongshe.com/reaction/11350
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | tert-butyl N-(4-aminobutyl)carbamate | HCID 4351 | — |
| 반응물 | 2,4-Dichloro-6-methyl-3-nitropyridine | HCID 2784819 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Tert-butyl 4-[(2-chloro-6-methyl-3-nitropyridin-4-yl)amino]butylcarbamate | HCID 12109135 | 98.5% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07098221B2 |
|---|
| 출처 데이터셋 | uspto-grants-2006_08 |
|---|
| ORD ID | ord-fded4986a54d42f184599c02d1ee8017 |
|---|
| 출처 메모 | uspto-grants-2006_08 |
|---|