HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Hydroxypyridazine-3-carboxylic Acid → 1,4,5,6-Tetrahydro-6-oxo-3-pyridazinecarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Hydroxypyridazine-3-carboxylic Acid | HCID 305970 | — |
| Reactant | 2,3,4-Trideutero-glutamine | HCID 86671832 | — |
| Product | 1,4,5,6-Tetrahydro-6-oxo-3-pyridazinecarboxylic acid | HCID 99621 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09290475B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-632db36a8d534b8ebe1258eaf1cf765a |
| Source note | uspto-grants-2016_03 |