Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043585Generated: November 4, 2026

2-(propan-2-yl)-1H-1,3-benzodiazole → (4-(2-hydroxypropan-2-yl)piperidin-1-yl)(2-(2-isopropyl-1H-benzo[d]imidazol-1-yl)-4-morpholinopyrido[3,2-d]pyrimidin-6-yl)methanone

https://huagongshe.com/reaction/1043585

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(propan-2-yl)-1H-1,3-benzodiazoleHCID 22121—
ReactantSodium t-butoxideHCID 23676156—
Reactant(2-Chloro-4-morpholinopyrido[3,2-d]pyrimidin-6-yl)(4-(2-hydroxypropan-2-yl)piperidin-1-yl)methanoneHCID 58404959—
Catalystpalladium(II) acetateHCID 167845—
CatalystHCID 178418851HCID 178418851—
Product(4-(2-hydroxypropan-2-yl)piperidin-1-yl)(2-(2-isopropyl-1H-benzo[d]imidazol-1-yl)-4-morpholinopyrido[3,2-d]pyrimidin-6-yl)methanoneHCID 53378372—

Reaction Steps

(2-Chloro-4-morpholinopyrido[3,2-d]pyrimidin-6-yl)(4-(2-hydroxypropan-2-yl)piperidin-1-yl)methanone from Example 118 (80 mg) was reacted with 2-isopropyl-1H-benzo[d]imidazole (1.05 eq), sodium tert-butoxide (2 eq), palladium acetate (0.1 eq) and bis(tri-t-butylphosphine)palladium (0.1 eq). The tube was flushed with nitrogen for 10 minutes before adding Toluene (2 mL). The reaction was microwaved at 145° C. for 20 minutes. The crude was loaded onto a Biotage isolute scx-2 cartridge, eluted with 2M ammonia in MeOH then purified by flash column chromatography to afford 6.6 mg of 119. MS (Q1) 544.3 (M)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563540B2
Source datasetuspto-grants-2013_10
ORD IDord-9d15f05f2d924414a1bf08154eed7669
Source noteuspto-grants-2013_10