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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297478Generated: October 30, 2026

Trifluoroacetic anhydride → HCID 18381604, compound

https://huagongshe.com/reaction/2297478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 53709462HCID 53709462—
SolventPyridineHCID 1049—
ProductHCID 18381604HCID 1838160433%

Reaction Steps

A solution of 4(3,5-dichloro-pyridin-4-ylmethyl)-7-methoxy-phthalazine-1-carboxylic acid amide (1.06 g, 2.92 mmoles), prepared as described in example 109, in pyridine (80 ml) and trifluoroacetic anhydride (1.65 ml, 11.67 mmoles), under dry N2 at room temperature, was stirred for 3 hours, then dried, taken up in CH2Cl2, washed with citric acid, 5% NaOH and water. The organic phase was anhydrified and dried to give a solid which was flash chromatographed (eluent: CH2Cl2/CH3OH 99:1) to give 0.33 g of the title compound (yield: 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492360B1
Source datasetuspto-grants-2002_12
ORD IDord-d7d99c9f0ed1417097ed539e75c11617
Source noteuspto-grants-2002_12