Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
6-Hydroxypyridazine-3-carboxylic Acid → 1,4,5,6-Tetrahydro-6-oxo-3-pyridazinecarboxylic acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 6-Hydroxypyridazine-3-carboxylic Acid | HCID 305970 | — |
| 반응물 | 2,3,4-Trideutero-glutamine | HCID 86671832 | — |
| 생성물 | 1,4,5,6-Tetrahydro-6-oxo-3-pyridazinecarboxylic acid | HCID 99621 | — |
반응 단계
A number of deuterated glutamines (starting material for preparing Compound B) have previously been made, including 2,3,4-trideutero-glutamine (i.e., R2=D, R4=D, and Z=D), which was made via the deuterium reduction of 6-carboxy-3(2H)-pyridazone (see Stogniew, J. Labelled Compounds and Radiopharmaceuticals 1981, 18(6), 897-903), and 2,2,3,3,4 pentadeutero-glutamine (i.e., R2-R5=D and Z=D), which was obtained in a multi-step synthesis (see Blomquist, J. Org. Chem. 1966, 12, 4121-27). Stogniew also notes that the 5-mono-deutero-glutamine could be obtained through deuterium reduction of 4,5-dihydro-6-carboxy-3(2H)-pyridazone.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09290475B2 |
| 출처 데이터셋 | uspto-grants-2016_03 |
| ORD ID | ord-632db36a8d534b8ebe1258eaf1cf765a |
| 출처 메모 | uspto-grants-2016_03 |