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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410099Generated: October 26, 2026

Cesium carbonate → Tert-butyl 1-(7-(5,6-dimethoxypyridin-2-ylamino)thiazolo[5,4-d]pyrimidin-5-yl)pyrrolidin-3-ylcarbamate

https://huagongshe.com/reaction/1410099

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactanttert-butyl N-(pyrrolidin-3-yl)carbamateHCID 2757234—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant5-chloro-N-(5,6-dimethoxypyridin-2-yl)thiazolo[5,4-d]pyrimidin-7-amineHCID 86671789—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
ProductTert-butyl 1-(7-(5,6-dimethoxypyridin-2-ylamino)thiazolo[5,4-d]pyrimidin-5-yl)pyrrolidin-3-ylcarbamateHCID 6837962151.8%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a stirred solution of 5-chloro-N-(5,6-dimethoxypyridin-2-yl)thiazolo[5,4-d]pyrimidin-7-amine (344 mg, 1.06 mmol), tert-butyl pyrrolidin-3-ylcarbamate (289 mg, 1.55 mmol), X-Phos (256 mg, 0.53 mmol) and Cs2CO3 (1.3 g, 3.9 mmol) in 120 mL of dioxane at room temperature under nitrogen was added Pd2(dba)3 (138 mg, 0.24 mmol) in one portion. Then the reaction was stirred at 95° C. under nitrogen for 24 hours. The solvent was evaporated and the residue was purified by silica gel chromatography (silica gel 200-300 mesh, eluting with a mixture of ethyl acetate and petroleum ether (2:1)) to give tert-butyl 1-(7-(5,6-dimethoxypyridin-2-ylamino)thiazolo[5,4-d]pyrimidin-5-yl)pyrrolidin-3-ylcarbamate (260 mg, 51.7%) as an oil. LC-MS: 474.2 [M+H]+, tR=1.67 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921383B2
Source datasetuspto-grants-2014_12
ORD IDord-c1e4efa11d6e4875b31bf370fe7a0517
Source noteuspto-grants-2014_12