HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → HCID 178433883, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | HCID 178433880 | HCID 178433880 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178433883 | HCID 178433883 | — |
Reaction Steps
3′-[(2Z)-[1-(3,4-dimethylphenyl)-1,5-dihydro-3-methyl-5-oxo-4H-pyrazol-4-ylidene]hydrazino]-2′-hydroxy-[1,1′-biphenyl]-3-carboxylic acid, 8 g of crude orange solid, was dissolved at room temperature in THF (240 ml) in a 500 ml round bottom 3-necked flask under a nitrogen atmosphere. Ethanolamine (2.2 ml, 2 molar equivalents) was added via syringe over 5 minutes. The resulting dark red suspension was stirred at room temperature for 1.5 hours and the solid isolated by filtration, washed with THF (16 ml×2) and dried at 50° C. in a vacuum oven over night to yield 10.37 g of the title compound (more than quantitative yield due to residual solvent—approximately 2.4% w/w THF as determined by NMR, otherwise similar to Example 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846024B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-7aa8e63d167945e2b4948e54805e61b6 |
| Source note | uspto-grants-2014_09 |