Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
N,N-Diisopropylmethylamine → (S)-1-methyl-N-(1-(1-phenyl-1H-benzo[d]imidazol-2-yl)ethyl)-1H-pyrazolo[4,3-d]pyrimidin-5-amine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | N,N-Diisopropylmethylamine | HCID 547370 | — |
| 반응물 | (S)-1-(1-Phenyl-1H-benzo[D]imidazol-2-YL)ethanamine | HCID 68157455 | — |
| 반응물 | 5-Chloro-1-methyl-1H-pyrazolo[4,3-D]pyrimidine | HCID 71743115 | — |
| 용매 | 1-Butanol | HCID 263 | — |
| 생성물 | (S)-1-methyl-N-(1-(1-phenyl-1H-benzo[d]imidazol-2-yl)ethyl)-1H-pyrazolo[4,3-d]pyrimidin-5-amine | HCID 68157281 | 35.9% |
반응 단계
A solution of (S)-1-(1-phenyl-1H-benzo[d]imidazol-2-yl)ethanamine from Example 4 (200 mg, 0.83 mmol, 1.00 equiv, 98%), 5-chloro-1-methyl-1H-pyrazolo[4,3-d]pyrimidine (180 mg, 1.07 mmol, 1.29 equiv) and methylbis(propan-2-yl)amine (0.3 mL, 98%) in n-butanol (8 mL) was stirred at 130° C. for 96 h. The resulting mixture was concentrated under vacuum and the residue was purified on a C18 column eluted with water/acetonitrile to give 110 mg (31%) of 159 as a light yellow solid. LC-MS: (ES, m/z) 370 [M+H]+, 221, 115. H-NMR: (CD3OD, 300 Hz, ppm) δ 8.86 (s, 1H), 7.70 (s, 1H), 7.65-7.54 (m, 6H), 7.61 (d, 2H), 7.09 (s, 1H), 5.30 (m, 1H), 4.04 (s, 3H), 1.64 (d, 3H)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08653089B2 |
| 출처 데이터셋 | uspto-grants-2014_02 |
| ORD ID | ord-f9003da174fb4f9e8742a63982d0cd83 |
| 출처 메모 | uspto-grants-2014_02 |