Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ammonium bifluoride → HCID 118380314, 화합물
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ammonium bifluoride | HCID 14935 | — |
| 반응물 | Cloperastine Hydrochloride | HCID 161104 | — |
| 반응물 | HCID 140689321 | HCID 140689321 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | HCID 22708839 | HCID 22708839 | — |
| 생성물 | HCID 118380314 | HCID 118380314 | 99.5% |
반응 단계
Prepared according to Seki et al. Synlett 1995, 609-611. To a solution of tert-butyl 2-(((Z)-(1-(2-((tert-butoxycarbonyl)amino)thiazol-4-yl)-2-(((2R,3S)-2-(((2-((tert-butyldimethylsilyl)oxy)ethyl)amino)methyl)-4-oxoazetidin-3-yl)amino)-2-oxoethylidene)amino)oxy)-2-methylpropanoate (111 mg, 0.162 mmol) in DMF:NMP (2.7:1, 1.62 mL) was added ammonium fluoride hydrofluoride (37.0 mg, 0.648 mmol). After stirring for 65 h, the solution was diluted with water and extracted with EtOAc. The organic layer was dried over sodium sulfate and concentrated in vacuo to afford crude title compound (92 mg, 99%). The crude material was used directly in step 3. LCMS: R=0.76 min, m/z 571.3 (M+1) Method 2m_acidic.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09174978B2 |
| 출처 데이터셋 | uspto-grants-2015_11 |
| ORD ID | ord-7dc75cf636b5476cab09d566abb21a73 |
| 출처 메모 | uspto-grants-2015_11 |