Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2-tert-Butyl-1,3-diisopropylisourea → 4-(4-Bromo-2-chlorophenylamino)-6-chloronicotinic acid tert-butyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2-tert-Butyl-1,3-diisopropylisourea | HCID 11041782 | — |
| 반응물 | 4-(4-Bromo-2-chlorophenylamino)-6-chloronicotinic acid hydrochloride salt | HCID 86596777 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 4-(4-Bromo-2-chlorophenylamino)-6-chloronicotinic acid tert-butyl ester | HCID 86596778 | 107.3% |
반응 단계
2-tert-Butyl-1,3-diisopropylisourea (8.04 g, 40.1 mmol) was added to a mixture of 4-(4-bromo-2-chlorophenylamino)-6-chloronicotinic acid hydrochloride salt (24) (2.91 g, 7.31 mmol) in THF (165 mL). After stirring for 2 hours at room temperature and 30 minutes at reflux, the reaction mixture was cooled to room temperature and diluted with EtOAc. The organic layer was washed with 10% K2CO3 and brine, dried (Na2SO4) and concentrated. The resulting residue was dissolved in CH2Cl2 and filtered. The filtrate was concentrated and purified by flash column chromatography using the Biotage system (CH2Cl2) to give the desired product (40) (3.28 g, 78%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07538120B2 |
| 출처 데이터셋 | uspto-grants-2009_05 |
| ORD ID | ord-b9925329c8134f9fbab4bddce9e963e1 |
| 출처 메모 | uspto-grants-2009_05 |