HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178433793, compound → HCID 178433795, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178433793 | HCID 178433793 | — |
| Reactant | HCID 178433813 | HCID 178433813 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178433795 | HCID 178433795 | 81.9% |
Reaction Steps
(Z)-5-{2-hydroxy-3-[N′-(1-indan-5-yl-3-methyl-5-oxo-1,5-dihydro-pyrazol-4-ylidene)-hydrazino]-phenyl}-furan-2-carboxylic acid 16a (150 mg, 0.38 mmol) was suspended in 5 mL of tetrahydrofuran to form a dark red suspension. The reaction mixture was added dropwise with diethylamine (49 mg, 0.67 mmol) to form a purple solution, and stirred for 2 hours at room temperature. The solid was precipitated from solution, filtered, then the filter cake was washed with tetrahydrofuran (1 mL×3) and dired in vacuo to obtain the title compound (Z)-5-{2-hydroxy-3-[N′-(1-indan-5-yl-3-methyl-5-oxo-1,5-dihydro-pyrazol-4-ylidene)-hydrazino]-phenyl}-furan-2-carboxylic acid bis-(diethylamine) 17 (163 mg, yield: 81.9%) as a dark red solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08642637B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-2f915dab99fc44768b7e5ceaaa186f67 |
| Source note | uspto-grants-2014_02 |