Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine hydrochloride → 6-Chloro-3-(2,6-difluorophenyl)-7-(1,1-dimethylethyl)-1,2,4-triazolo[4,3-b]pyridazine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine hydrochloride | HCID 11130 | — |
| 반응물 | 4-tert-Butyl-3,6-dichloropyridazine | HCID 89846 | — |
| 반응물 | 2,6-Difluorobenzhydrazide | HCID 676449 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 6-Chloro-3-(2,6-difluorophenyl)-7-(1,1-dimethylethyl)-1,2,4-triazolo[4,3-b]pyridazine | HCID 18372415 | 13.3% |
반응 단계
A mixture of 3,6-dichloro-4-(1,1-dimethylethyl)pyridazine (2 g, 9.75 mmol), 2,6-difluorobenzoic acid hydrazide (2.52 g, 14.6 mmol) (WO 95/24403) and triethylamine hydrochloride (2.01 g, 14.6 mmol) in 1,4-dioxane (10 ml) was stirred and heated at reflux for 3.5 days. Upon cooling, the volatiles were removed in vacuo and the residue was triturated with dichloromethane. Any undissolved solid was removed by filtration. The residue was purified by chromatography on silica gel eluting with 0%→25% ethyl acetate in dichloromethane to give the required product (0.42 g). Data for the title compound: 1H NMR (250 MHz, CDCl3) δ1.57 (9H, s), 7.09-7.16 (2H, m), 7.51-7.63 (1H, m), 8.19 (1H, s); MS (ES30) m/e 323 (MH+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06500828B1 |
| 출처 데이터셋 | uspto-grants-2002_12 |
| ORD ID | ord-34c2f76c0c3849799ce74e5dab82164e |
| 출처 메모 | uspto-grants-2002_12 |