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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657592Generated: October 30, 2026

Trifluoroacetic acid → HCID 25230871, compound

https://huagongshe.com/reaction/657592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 57624578HCID 57624578—
SolventDichloromethaneHCID 6344—
ProductHCID 25230871HCID 2523087186%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of phosphoric acid di-tert-butyl ester 3-[2,6-dichloro-4-(6-cyano-3,5-dioxo-4,5-dihydro-3H-[1,2,4]triazin-2-yl)-phenoxy]-5-isopropyl-6-oxo-6H-pyridazin-1-ylmethyl ester (44.0 mg, 0.067 mmol) in methylene chloride (1.0 mL, 0.067M) at 25° C. was treated with trifluoroacetic acid (0.2 mL). The reaction mixture was stirred at 25° C. for 20 min. At this time, the reaction mixture was concentrated in vacuo, azeotropically dried with benzene and concentrated from absolute ethanol followed by lyophilization from acetonitrile and water to afford phosphoric acid mono-{3-[2,6-dichloro-4-(6-cyano-3,5-dioxo-4,5-dihydro-3H-[1,2,4]triazin-2-yl)-phenoxy]-5-isopropyl-6-oxo-6H-pyridazin-1-ylmethyl}ester (31.4 mg, 86%) an off-white solid. Present in the product was 0.95 moles of residual ammonium from the ammonium acetate used in the supercritical fluid purification of the precursor. ES+-HRMS m/e calcd for C18H15N6O8PCl2 (M+Na+) 566.9958, found 566.9962.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076334B2
Source datasetuspto-grants-2011_12
ORD IDord-e01a65ad82484e87a3f166c7ec74623b
Source noteuspto-grants-2011_12