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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1529458Generated: November 2, 2026

2-Bromothiazole → HCID 67959986, compound

https://huagongshe.com/reaction/1529458

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromothiazoleHCID 76430—
ReactantHCID 67960651HCID 67960651—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
ProductHCID 67959986HCID 6795998622.2%

Reaction Steps

A solution of 2-bromothiazole (20 mg, 0.12 mmol) and benzyl trans-4-fluoro-3-((4-((4-methoxybenzyl)oxy)-6-(1-(tetrahydro-2H-pyran-2-yl)-5-(trimethylstannyl)-1H-indazol-3-yl)pyrimidin-2-yl)oxy)piperidine-1-carboxylate (racemic) (100 mg, 0.12 mmol) in DMF (1 mL) was bubbled with argon for 15 min. To the above mixture was added CuI (11 mg, 0.060 mmol) and Pd(PPh3)4 (13 mg, 0.012 mmol) and argon gas was bubbled for another 15 min. The reaction was heated at 100 C for 2 h. The reaction was quenched with water and the suspension was filtered. The solid was dried then purified with basic alumina chromatography (eluting with 30% EtOAc in hexanes) to give benzyl trans-4-fluoro-3-((4-((4-methoxybenzyl)oxy)-6-(1-(tetrahydro-2H-pyran-2-yl)-5-(thiazol-2-yl)-1H-indazol-3-yl)pyrimidin-2-yl)oxy)piperidine-1-carboxylate (racemic) (20 mg, 11%) as a off brown solid. MS (ESI, pos. ion) m/z: 750.8 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090593B2
Source datasetuspto-grants-2015_07
ORD IDord-dbe6c488827646ee85f766bf0cb09eac
Source noteuspto-grants-2015_07