Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Benzenamine, 3-chloro-, hydrochloride (1:1) → 4-(3-chloro-phenylamino)-3-(4-tert-butyloxycarbonyl-piperazin-1-yl)-1H-pyrazolo[3,4-d]pyrimidine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Benzenamine, 3-chloro-, hydrochloride (1:1) | HCID 67336 | — |
| 반응물 | N'-[3-(4-tert-butoxycarbonyl-piperazin-1-yl)-4-cyano-1H-pyrazol-5-yl]-N,N-dimethyl-formamidine | HCID 54424143 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 4-(3-chloro-phenylamino)-3-(4-tert-butyloxycarbonyl-piperazin-1-yl)-1H-pyrazolo[3,4-d]pyrimidine | HCID 21190607 | — |
반응 단계
With the exclusion of air, 16.2 9 (46.6 mmol) of N′-[3-(4-tert-butoxycarbonyl-piperazin-1 -yl)-4-cyano-1H-pyrazol-5-yl]-N,N-dimethyl-formamidine in 130 ml methanol are heated to boiling with 11.47 g (70 mmol) of 3-chloro-aniline hydrochloride. After 9 hours the reaction mixture is cooled, filtered and washed with methanol and DIPE. Stirring the crude product in boiling ethanol, cooling and filtration yield 4-(3-chloro-phenylamino)-3-(4-tert-butyloxycarbonyl-piperazin-1-yl)-1H-pyrazolo[3,4-d]pyrimidine; HPLC: tRet(grad20-100/20)=15.7; IR (KBr) interalia 1706 s, 1631 s, 1610 s, 1589 s, 1508 m, 1482 s, 1425 m, 1364 m, 1304 m, 1283 m, 1245 m, 1170 m, 1122 m.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06251911B1 |
| 출처 데이터셋 | uspto-grants-2001_06 |
| ORD ID | ord-0c6a5e6e8741484384f1f6d5cd40256e |
| 출처 메모 | uspto-grants-2001_06 |