Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → (4R)-N-[(1S)-1-Methyl-2-hydroxyethyl]-2-oxothiazolidin-4-yl-carboxamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Procysteine | HCID 72390 | — |
| 반응물 | L-Alaninol | HCID 80307 | — |
| 반응물 | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (4R)-N-[(1S)-1-Methyl-2-hydroxyethyl]-2-oxothiazolidin-4-yl-carboxamide | HCID 21309140 | 66.3% |
반응 단계
In 20 ml of dry tetrahydrofuran were dissolved 1.0 g of (4R)-2-oxothiazolidine-4-carboxylic acid and 0.56 g of L-alaninol, 2.8 ml of triethylamine and 1.8 ml of diphenylphosphoryl azide were added thereto with stirring under ice-cooling, and the mixture was stirred at room temperature for 3 hours. Then, the solvent was distilled off under reduced pressure and the obtained residue was purified by silica gel column chromatography employing ethyl acetate as an eluent and further purified by silica gel column chromatography employing dichloromethane-methanol (95:5) as an eluent to obtain 0.92 g of the desired compound as colorless crystals.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05891898 |
| 출처 데이터셋 | uspto-grants-1999_04 |
| ORD ID | ord-91ff4ee8f9bc4b65ad9810482c255100 |
| 출처 메모 | uspto-grants-1999_04 |