참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethanolamine | HCID 700 | — |
| 반응물 | Nicotinate | HCID 937 | — |
| 반응물 | N-Hydroxysuccinimide | HCID 80170 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | N-succinimidyl-nicotinate | HCID 86742329 | — |
| 반응물 | ethylamine DMF | HCID 86742330 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | N-(2-hydroxyethyl)nicotinamide | HCID 72663 | — |
반응 단계
The N-succinimidyl-nicotinate compound described in Example 1 was reacted with the hydrochloric salt of ethanolamine, available commercially in its radioactive form. The ethanolamine salt was dissolved in dried DMF and chilled in an ice bath. To the mixture was added an equimolar of diisopropylethylamine (DIEA) and stirred for 15 minutes. An equimolar solution of N-succinimidyl-nicotinate was added to the ethylamine-DMF mixture dropwise under a nitrogen atmosphere. As the nicotinate was added the mixture turned milky and was slurried for at least another half hour. The milky substance was the N-hydroxy-succinimide precipitating, which was filtered off. The DMF-mixture was washed with ether to remove any precipitant. The solvent mixture was removed under high vaccum. The oily mixture was triturated with ether to yield a precipitant, N-(2-hydroxyethyl)nicotinamide. The radioactive compound was isolated and identified by its TLC.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04764462 |
|---|
| 출처 데이터셋 | uspto-grants-1988_08 |
|---|
| ORD ID | ord-b5b09e4205d74d908c6d4d8044e0f888 |
|---|
| 출처 메모 | uspto-grants-1988_08 |
|---|