Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
N-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide ester → 5-Amino-4-[2-(tert-butoxycarbonylamino)acetyl]amino-1-(2-hydroxyethyl)pyrazole
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | N-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide ester | HCID 76926 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 4,5-Diamino-1-(2-hydroxyethyl)pyrazole sulfate | HCID 11673148 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 5-Amino-4-[2-(tert-butoxycarbonylamino)acetyl]amino-1-(2-hydroxyethyl)pyrazole | HCID 21904515 | 80.8% |
반응 단계
To a suspension of 4,5-diamino-1-(2-hydroxyethyl)pyrazole sulfuric acid salt (1.20 g) and N-[2-(tert-butoxycarbonylamino)acetoxy]succinimide (1.35 g) in methylene chloride (20 ml) was added N-ethyldiisopropylamine (2.1 ml) under ice-cooling, and the mixture was stirred at room temperature for 17 hours. The reaction mixture was washed with water (40 ml), saturated aqueous sodium hydrogen carbonate solution (40 ml) and brine (40 ml). The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The oily residue was purified by column chromatography on silica gel eluting with 10% methanol/chloroform to give 5-amino-4-[2-(tert-butoxycarbonylamino)acetyl]amino-1-(2-hydroxyethyl)pyrazole (1.20 g) as a solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07129232B2 |
| 출처 데이터셋 | uspto-grants-2006_10 |
| ORD ID | ord-52dd1d3126c343a9b2cb3cf6af9914c6 |
| 출처 메모 | uspto-grants-2006_10 |