HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271457Generated: November 2, 2026
HCID 178433821, compound → HCID 178433823, compound
https://huagongshe.com/reaction/2271457
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178433821 | HCID 178433821 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178433823 | HCID 178433823 | 72.8% |
Reaction Steps
(Z)-4-(2-hydroxy-3-{N′-[3-methyl-5-oxo-1-(5,6,7,8-tetrahydro-naphthal-2-yl)-1,5-dihydro-pyrazol-4-ylidene]-hydrazino}-phenyl)-furan-2-carboxylic acid 22f (1.2 g, 2.6 mmol) was dissolved in 20 mL of tetrahydrofuran to form a dark red suspension. The reaction mixture was added with ethanolamine (399 mg, 6.5 mmol) to form a purple solution, and stirred for 6 hours at room temperature. A great quantity of the solid was precipitated from the solution, filtered, then the filter cake was washed with tetrahydrofuran (1 mL×3) and dried in vacuo to obtain the title compound (Z)-4-(2-hydroxy-3-{N′-[3-methyl-5-oxo-1-(5,6,7,8-tetrahydro-naphthal-2-yl)-1,5-dihydro-pyrazol-4-ylidene]-hydrazino}-phenyl)-furan-2-carboxylic acid bis-(ethanolamine) 22 (1.51 g, as a red solid) yield 72.8%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09120762B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-535331dead354691abd4e1c8da33759c |
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| Source note | uspto-grants-2015_09 |
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