Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Phosgene → N-[N-(1-Carboxy-3-phenylpropyl)-alpha-azaglycinyl]-4(R)carboethoxy-2-(2-hydroxyphenyl)thiazolidine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Phosgene | HCID 6371 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | HCID 20223100 | HCID 20223100 | — |
| 반응물 | ethyl (4R)-2-(2-hydroxyphenyl)-4-thiazolidinecarboxylate | HCID 54389765 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-[N-(1-Carboxy-3-phenylpropyl)-alpha-azaglycinyl]-4(R)carboethoxy-2-(2-hydroxyphenyl)thiazolidine | HCID 18606071 | — |
반응 단계
An ice-cold solution of phosgene (1.1 M solution in toluene; 0.91 ml) was diluted with CH2Cl2 (3 ml) and then a solution of 56 (0.34 g, 1.0 mmol) and triethylamine (0.28 ml; 2.0 mmol) in CH2Cl2 (3 ml) was added slowly with cooling (ice-bath). Then a solution of 57 (0.25 g; 1.0 mmol) and triethyl amine (0.14 ml; 1.0 mmol) in CH2Cl2 (3 ml) was added and stirring was continued at room temperature for 6 hours. The reaction mixture was diluted with EtAc (25 ml) and extracted with H2O (2×10 ml) and brine, and dried (MgSO4). The residue after evaporation was subjected to chromatography on silica gel, allowing isolation of 58.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04634715 |
| 출처 데이터셋 | uspto-grants-1987_01 |
| ORD ID | ord-29a584bcb1b84508a98d4a90b9654777 |
| 출처 메모 | uspto-grants-1987_01 |