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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513792Generated: October 29, 2026

Pyrrolidine → 12-Pyrrolidin-1-yl-5H-6-thia-4,5-diaza-chrysene 6,6-dioxide

https://huagongshe.com/reaction/513792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant12-bromo-5H-6-thia-4,5-diaza-chrysene 6,6-dioxideHCID 16759944—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
Product12-Pyrrolidin-1-yl-5H-6-thia-4,5-diaza-chrysene 6,6-dioxideHCID 6818329534%

Reaction Conditions

Temperature90 °C

Reaction Steps

Toluene was de-gassed for 15 min. Toluene (2 ml) and pyrrolidine (30 μl, 0.42 mmol) were added to a mixture of Pd2(dba)3 (25 mg, 28 μmol), X-Phos (66 mg, 0.14 mmol), NaOtBu (67 mg, 0.69 mmol), 12-bromo-5H-6-thia-4,5-diaza-chrysene 6,6-dioxide 545 (100 mg, 0.28 mmol), under nitrogen and the mixture was heated at 90° C. for 18 h. After cooling, the mixture was diluted with MeOH (3 ml), filtered and concentrated in vacuo. The residue was purified by preparative HPLC (acidic conditions 1) to give the title compound (33 mg, 34%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102688B2
Source datasetuspto-grants-2015_08
ORD IDord-d3dc4a5da2bd45b89b92961771a6ed53
Source noteuspto-grants-2015_08