Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methylamine → 2-chloro-N-methyl-5-nitropyrimidin-4-amine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methylamine | HCID 6329 | — |
| 반응물 | 2,4-Dichloro-5-nitropyrimidine | HCID 521266 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-chloro-N-methyl-5-nitropyrimidin-4-amine | HCID 7147232 | 99.3% |
반응 단계
A solution of 2,4-dichloro-5-nitropyrimidine (7.26 g, 37.4 mmol) in THF (100 ml) is cooled to −78° C. A solution of methyl amine (8 M in methanol, 9.35 mL, 74.8 mmol) is added dropwise. The mixture is allowed to warm to room temperature, and concentrated. The residue is partitioned between ethyl acetate and water. The layer is separated and the aqueous layer is extracted with ethyl acetate. The combined organic extracts are washed with brine, dried over Na2SO4, filtered and concentrated to afford the title product (7.0 g). (Note: the product contains 5% regio-isomer, 4-chloro-2-(methylamino)-5-nitropyrimidine). The residue is used in the next step without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07423038B2 |
| 출처 데이터셋 | uspto-grants-2008_09 |
| ORD ID | ord-83d91350d3d04fa4bc5182a219334930 |
| 출처 메모 | uspto-grants-2008_09 |