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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676351Generated: October 31, 2026

Trifluoroacetic acid → HCID 58949484, compound

https://huagongshe.com/reaction/1676351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-butyl 4-(7-(2-fluoro-4-(2-(4-fluorophenyl)-3-oxo-2,3-dihydropyridazine-4-carboxamido)phenoxy)thieno[3,2-b]pyridin-2-yl)-5,6-dihydropyridine-1(2H)-carboxylateHCID 67346517—
ProductHCID 58949484HCID 5894948472.2%

Reaction Steps

A single-neck, round-bottomed flask was charged with tert-butyl 4-(7-(2-fluoro -4-(2-(4-fluorophenyl)-3-oxo-2,3-dihydropyridazine-4-carboxamido)phenoxy)thieno[3,2-b]pyridin-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate (27.3 mg, 0.0415 mmol) and CF3CO2H (5 mL). The reaction mixture was stirred at room temperature until the starting material had been consumed (four hours). Then the solvent was removed and the residue was purified by silica gel chromatography (DCM/7 M NH3 in MeOH from 50/1 to 10/1, v/v) to afford product (16.7 mg, 72.2%). LRMS (APCI pos): >99% purity, 254 nm, m/e 558 (M+1). 1H NMR (400 MHz, CDCl3) δ 11.83 (s, 1H), 8.42 (m, 2H), 8.24 (d, 1H), 7.95 (dd, 1H), 7.60 (m, 2H), 7.38 (m, 2H), 7.24 (m, 3H), 6.48 (d, 1H), 6.40 (s, 1H), 3.59 (m, 2H), 3.15 (m, 2H), 2.58 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003662B2
Source datasetuspto-grants-2011_08
ORD IDord-d7ddd4be36af4e2193d4917583eacb71
Source noteuspto-grants-2011_08