Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707476Generated: October 26, 2026

Toluene → benzyl N-[2-[8-[(4-methoxyphenyl)methyl]-7-oxo-3,5,6,8,10-pentazatricyclo[7.4.0.02,6]trideca-1(9),2,4,10,12-pentaen-12-yl]ethyl]carbamate

https://huagongshe.com/reaction/707476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantCesium carbonateHCID 10796—
ReactantPotassium benzyl N-[2-(trifluoroboranuidyl)ethyl]carbamateHCID 49761741—
Reactant9-bromo-6-(4-methoxybenzyl)pyrido[3,2-e][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)-oneHCID 86705385—
SolventWaterHCID 962—
Productbenzyl N-[2-[8-[(4-methoxyphenyl)methyl]-7-oxo-3,5,6,8,10-pentazatricyclo[7.4.0.02,6]trideca-1(9),2,4,10,12-pentaen-12-yl]ethyl]carbamateHCID 11811603012%

Reaction Conditions

Temperature80 °C

Reaction Steps

9-Bromo-6-(4-methoxybenzyl)pyrido[3,2-e][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)-one (30 mg, 0.078 mol), potassium (2-(benzyloxycarbonylamino)ethyl)trifluoroborate (30 mg, 0.11 mol), cesium carbonate (122 mg, 0.38 mmol), [1,1′-bis(diphenylphosphino)ferrocene]-dichloropalladium(II) DCM complex (5 mg, 0.01 mol), toluene (0.75 ml) and degassed water (0.25 ml) were added in order. The mixture was heated at 80° C. for 16 hours, concentrated under a stream of nitrogen, diluted with DMF (1.5 mL), filtered and purified by HPLC to afford 6 mg (12%) of 204 as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09175010B2
Source datasetuspto-grants-2015_11
ORD IDord-c795aaf2365c4fc7a671eebc0e7d7320
Source noteuspto-grants-2015_11