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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626635Generated: November 1, 2026

(S)-tert-butyl 2-(4-(3-ethylureido)phenyl)-4-(3-methylmorpholino)-5,6-dihydropyrido[3,4-d]pyrimidine-7(8H)-carboxylate → (S)-ethyl 4-(3-methylmorpholino)-2-(4-(3-(pyridin-4-yl)ureido)phenyl)-5H-pyrrolo[3,4-d]pyrimidine-6(7H)-carboxylate

https://huagongshe.com/reaction/1626635

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-tert-butyl 2-(4-(3-ethylureido)phenyl)-4-(3-methylmorpholino)-5,6-dihydropyrido[3,4-d]pyrimidine-7(8H)-carboxylateHCID 59239149—
Reactant1-(Pyridin-4-yl)-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ureaHCID 66687800—
ReactantHCID 86663155HCID 86663155—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Product(S)-ethyl 4-(3-methylmorpholino)-2-(4-(3-(pyridin-4-yl)ureido)phenyl)-5H-pyrrolo[3,4-d]pyrimidine-6(7H)-carboxylateHCID 6667895249%

Reaction Steps

Method as described for intermediate 5 using (S)-ethyl 2-chloro-4-(3-methylmorpholino)-5H-pyrrolo[3,4-d]pyrimidine-6(7H)-carboxylate (intermediate 11) and 1-(pyridin-4-yl)-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea as starting materials and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) as catalyst. The mixture was filtered through a celite 545 pre-packed cartridge (2.5 g), washed with MeOH and solvent removed in vacuo. The residue was purified by prep HPLC (low pH) yielding the title compound (38.2 mg, 0.08 mmol, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785457B2
Source datasetuspto-grants-2014_07
ORD IDord-1a02fa93649044f0946c4d055b5e6e32
Source noteuspto-grants-2014_07