Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Glycine, N-(3-nitrobenzoyl)- → N-[2-[[(3-nitrophenyl)carbonyl]amino]-1-oxoethyl]-beta-alanine, ethyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Glycine, N-(3-nitrobenzoyl)- | HCID 94858 | — |
| 반응물 | beta-Alanine, ethyl ester, hydrochloride | HCID 458475 | — |
| 반응물 | Di(succinimido) carbonate | HCID 676246 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Potassium Carbonate | HCID 11430 | — |
| 생성물 | N-[2-[[(3-nitrophenyl)carbonyl]amino]-1-oxoethyl]-beta-alanine, ethyl ester | HCID 20745455 | 97% |
반응 단계
N,N'-Disuccinimidyl carbonate (14 g, 5.5 mmol) was added to 3-nitrobenzoyl glycine (10 g, 4.5 mmol) of Example BB in dry dimethylformamide (30 mL) followed by N,N-dimethylaminopyridine (200 mg). After a period of 1 hour beta-alanine ethyl ester hydrochloride (7 g, 4.6 mmol) in 20% aqueous potassium carbonate (50 mL) was added in one portion. After complete reaction the product was collected by filtration (14 g, 97% yield). 1H-NMR (d6 -DMSO) δ, 1.18 (t, 3H, J=7.2 Hz), 2.46 (t, 2H, J=7.0), 3.34 (q, 2H, J1 =6.7 Hz, J2 =12.6 Hz), 3.87 (d, 2H, J=5.9 Hz), 4.05 (q, 2H, J1 =7.4 Hz, J2 =14.2 Hz), 7.8 (t, 1H, J=8.0 Hz), 8.1 (t, 1H, J=5.6 Hz), 8.35 (m, 2H), 8.71 (s, 1H), 9.22 (bs, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06028223 |
| 출처 데이터셋 | uspto-grants-2000_02 |
| ORD ID | ord-1ad9e99276204fa9a22f72084a62afcc |
| 출처 메모 | uspto-grants-2000_02 |