Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Tributylphosphine → 5-chloro-3-(3-chlorobenzyl)-N-[1-(4-cyanophenyl)ethyl]thiophene-2-carboxamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Tributylphosphine | HCID 13831 | — |
| 반응물 | Diphenyl diselenide | HCID 15460 | — |
| 반응물 | 4'-Cyanoacetophenone | HCID 74044 | — |
| 반응물 | HCID 45140204 | HCID 45140204 | — |
| 반응물 | HCID 57900982 | HCID 57900982 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 5-chloro-3-(3-chlorobenzyl)-N-[1-(4-cyanophenyl)ethyl]thiophene-2-carboxamide | HCID 57900981 | — |
반응 단계
To a suspension of 5-chloro-3-(3-chlorobenzyl)thiopbene-2-carboxylic acid from Example 1, Step 6 (230 mg, 0.801 mmol), 4-(1-azidoethyl)benzonitrile (146 mg, 0.848 mmol) [prepared according to Thompson et al. J. Org. Chem. 1993, 58, 5886, after reduction of commercially available 4-acetylbenzonitrile] and diphenyl diselenide (549 mg, 1.76 mmol) in acetonitrile at r.t. under N2 was added tributylphosphine (217 μL, 0.881 mmol, 1.1 eq) dropwise (suspension dissolved, slightly exothermic) and the mixture was stirred at r.t. for 6 h, quenched with saturated NaHCO3 and extracted with ether. The crude was purified by Combi Flash chromatography system (10-40% EtOAc/hexane) to give the desired product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08969394B2 |
| 출처 데이터셋 | uspto-grants-2015_03 |
| ORD ID | ord-27512fc6ee68476f8bc87d3b9152fbd4 |
| 출처 메모 | uspto-grants-2015_03 |