Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-Amino-3-fluorobenzoic acid → 4-amino-N-(1-ethylpiperidin-4-yl)-3-fluorobenzamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-Amino-3-fluorobenzoic acid | HCID 9971 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 1-Ethylpiperidin-4-amine | HCID 3734990 | — |
| 반응물 | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| 용매 | Dimethylacetamide | HCID 31374 | — |
| 생성물 | 4-amino-N-(1-ethylpiperidin-4-yl)-3-fluorobenzamide | HCID 55102782 | 22.7% |
반응 단계
4-amino-3-fluorobenzoic acid (2.115 g, 13.6 mmol), 4-Amino-1-Ethyl Piperidine (Fluorochem; 1.923 g, 15 mmol), HATU (5.7 g, 15 mmol) and DIPEA (7.1 mL, 40.8 mmol) were combined in DMA (60 mL) and the resulting yellow solution stirred at room temperature for 20 minutes. The reaction was left over the weekend at room temperature, solvent evaporated and the residue dissolved in methanol (10 mL) and loaded onto an SCX-2 column (50 g) which pre-wet with MeOH (40 mL), flushed with MeOH (4×30 ml) and eluted with 7N ammonia in MeOH (4×30 mL). Product containing, ammoniacal fractions were combined to yield the title compound as a brown solid (0.819 g, 22%)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07709471B2 |
| 출처 데이터셋 | uspto-grants-2010_05 |
| ORD ID | ord-60cb88dc051744b899d25578ed6a4372 |
| 출처 메모 | uspto-grants-2010_05 |