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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400918Generated: October 27, 2026

Phenolate → tert-butyl 4-(2-(4-(7-(4-amino-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)-1H-imidazol-1-yl)ethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1400918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolateHCID 119047—
ReactantPhenol, 4-amino-2-fluoro-HCID 2735918—
Reactant4-Amino-2-fluorophenol hydrochlorideHCID 19599201—
ReactantPotassium tert-butoxideHCID 23665647—
Reactanttert-butyl 4-(2-(4-(7-chlorothieno[3,2-b]pyridin-2-yl)-1H-imidazol-1-yl)ethyl)piperazine-1-carboxylateHCID 67442621—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Producttert-butyl 4-(2-(4-(7-(4-amino-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)-1H-imidazol-1-yl)ethyl)piperazine-1-carboxylateHCID 6744215647%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of 4-amino-2-fluorophenol x HCl (1.64 g, 10.05 mmol) in NMP (30 mL) was added t-BuOK (2.25 g, 20.1 mmol). After 30 min, compound 305 (3.75 g, 8.37 mmol) was added and the reaction mixture was heated at 100° C. for 1 h. A solution of 4-amino-2-fluorophenol HCl (1.64 g, 10.05 mmol) in NMP (30 mL) in a separate flask was treated with t-BuOK (2.25 g, 20.1 mmol) and the resultant phenolate solution was added to the reaction mixture at 100° C. After 30 min, the reaction was quenched by addition of water and the precipitate was collected by filtration, dried and triturated with MTBE to afford the title compound 306 (2.10 g, 3.90 mmol, 47% yield) as a beige solid. MS (m/z): 539.39 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906852B2
Source datasetuspto-grants-2014_12
ORD IDord-adfe92d5b6324b769324c96a74dca69d
Source noteuspto-grants-2014_12