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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676368Generated: October 30, 2026

4-(7-(4-amino-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)-N-methylbenzamide → 4-(7-(2-Fluoro-4-(1-(4-fluorophenyl)-6-oxo-1,6-dihydropyridazine-5-carboxamido)phenoxy)thieno[3,2-b]pyridin-2-yl)benzoic acid

https://huagongshe.com/reaction/1676368

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(7-(4-amino-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)-N-methylbenzamideHCID 67348698—
Reactant1-((4-Fluorophenyl)carbamoyl)cyclopropanecarbonyl fluorideHCID 86614649—
Reactant2-(4-Fluorophenyl)-3-oxo-2,3-dihydropyridazine-4-carbonyl fluorideHCID 86614653—
SolventWaterHCID 962—
Product4-(7-(2-Fluoro-4-(1-(4-fluorophenyl)-6-oxo-1,6-dihydropyridazine-5-carboxamido)phenoxy)thieno[3,2-b]pyridin-2-yl)benzoic acidHCID 67345297—

Reaction Steps

Prepared according to the procedure for Example 112, Step B substituting 4-(7-(4-amino-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)benzoic acid (1.25 g, 3.29 mmol) for 4-(7-(4-amino-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)-N-methylbenzamide and 2-(4-fluorophenyl)-3-oxo-2,3-dihydropyridazine-4-carbonyl fluoride (1.70 g, 5.75 mmol) for 1-((4-fluorophenyl)carbamoyl)cyclopropanecarbonyl fluoride. When the reaction was complete, water (20 mL) was added and the product (1.59 g, 80%) was collected by filtration to get a brown solid. LRMS (esi+) 597 m/z (M+1) detected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003662B2
Source datasetuspto-grants-2011_08
ORD IDord-ac1e1f7b52174f83a83d7153cffcfe2a
Source noteuspto-grants-2011_08