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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821420Generated: November 3, 2026

Triethylamine → HCID 69005019, compound

https://huagongshe.com/reaction/1821420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Nitrophthalic anhydrideHCID 21631—
ReactantHCID 68998211HCID 68998211—
SolventO-XyleneHCID 7237—
ProductHCID 69005019HCID 69005019—

Reaction Conditions

Temperature140 °C

Reaction Steps

To 3-amino-4-[2-(1H-indazol-3-yl)vinyl]benzoic acid (1.7 g, 6.2 mmol) obtained in Step 2 of Example 276, xylene (55 mL), triethylamine (0.45 mL, 3.1 mmol), 3-nitrophthalic anhydride (1.4 g, 7.4 mmol), molecular sieves 3A (2.0 g) were added, followed by heating at 140° C. for 4 hours. Molecular sieves 3A was filtered off and the reaction mixture was acidified by hydrochloric acid (2 mol/L). The precipitated crystal was collected by filtration to obtain (E)-4-[2-(1H-indazol-3-yl)vinyl]-3-(4-nitro-1,3-dioxo-1,3-dihydroisoindol-2-yl)benzoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605272B2
Source datasetuspto-grants-2009_10
ORD IDord-20870e22fccb4ad1919f090cc96e9620
Source noteuspto-grants-2009_10