Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238713Generated: October 29, 2026

HCID 178433793, compound → HCID 178433795, compound

https://huagongshe.com/reaction/238713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178433793HCID 178433793—
ReactantHCID 178433813HCID 178433813—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178433795HCID 17843379581.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642637B2
Source datasetuspto-grants-2014_02
ORD IDord-2f915dab99fc44768b7e5ceaaa186f67
Source noteuspto-grants-2014_02