Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydrochloric Acid → 5-Bromo-n4-isopropyl-n2-(4-methylsulphanylphenyl)pyrimidine-2,4-diamine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | chloramine-T trihydrate | HCID 517414 | — |
| 반응물 | 5-Bromo-n4-isopropyl-n2-(4-methyl-sulphanylphenyl)pyrimidine-2,4-diamine | HCID 131728842 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 5-Bromo-n4-isopropyl-n2-(4-methylsulphanylphenyl)pyrimidine-2,4-diamine | HCID 59674070 | — |
반응 단계
1.36 g (4.8 mmol) of chloramine-T trihydrate (Aldrich) are added to a suspension of 1.56 g (4.0 mmol) of the hydrochloride of 5-bromo-N4-isopropyl-N2-(4-methyl-sulphanylphenyl)pyrimidine-2,4-diamine in 20 ml of acetonitrile at room temperature. The mixture is stirred at room temperature for 16 hours and then diluted with ethyl acetate. The mixture is filtered with suction and the filter cake is washed with ethyl acetate. The combined organic phases are dried (Na2SO4), filtered and concentrated. The resulting residue is purified by HPLC:
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07943629B2 |
| 출처 데이터셋 | uspto-grants-2011_05 |
| ORD ID | ord-038419359e4a4eff90deb757ec39e87f |
| 출처 메모 | uspto-grants-2011_05 |