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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246529Generated: October 30, 2026

Cesium carbonate → tert-butyl 3-((3-(7-(tert-butylcarbamoyl)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazin-2-yl)-5-(difluoromethoxy)-1H-indazol-1-yl)methyl)azetidine-1-carboxylate

https://huagongshe.com/reaction/246529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactanttert-Butyl 3-(iodomethyl)azetidine-1-carboxylateHCID 53249943—
Reactant2-(5-difluoromethoxy-1H-indazol-3-yl)-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid tert-butylamideHCID 71279566—
SolventDimethylformamideHCID 6228—
Producttert-butyl 3-((3-(7-(tert-butylcarbamoyl)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazin-2-yl)-5-(difluoromethoxy)-1H-indazol-1-yl)methyl)azetidine-1-carboxylateHCID 71280303—

Reaction Steps

N-tert-Butyl-2-(5-(difluoromethoxy)-1H-indazol-3-yl)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (152 mg, 286 μmol), tert-butyl 3-(iodomethyl)azetidine-1-carboxylate (85.1 mg, 286 μmol) and cesium carbonate (280 mg, 859 μmol) in dimethylformamide (3 mL) were heated in a microwave at 150° C. for 30 min. The mixture was partitioned between ethyl acetate and water, washed with water, dried and concentrated in vacuo. Purification by chromatography (silica, 24 g Analogix column, 0-40% ethyl acetate in hexanes) gave tert-butyl 3-((3-(7-(tert-butylcarbamoyl)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazin-2-yl)-5-(difluoromethoxy)-1H-indazol-1-yl)methyl)azetidine-1-carboxylate that was used directly without purification. MS (M+H)+=702.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-3020fcf028ff4a2a9a5ee2b7cef213e5
Source noteuspto-grants-2014_02