HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657592Generated: October 30, 2026
Trifluoroacetic acid → HCID 25230871, compound
https://huagongshe.com/reaction/657592
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 57624578 | HCID 57624578 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 25230871 | HCID 25230871 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08076334B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-e01a65ad82484e87a3f166c7ec74623b |
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| Source note | uspto-grants-2011_12 |
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