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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697899Generated: October 31, 2026

Potassium Iodide → (S)-2-(2-(4-(3-ethylureido)phenyl)-4-(3-methylmorpholino)-5,6-dihydropyrido[3,4-d]pyrimidin-7(8H)-yl)-N,N-dimethylacetamide

https://huagongshe.com/reaction/1697899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant2-chloro-N,N-dimethylacetamideHCID 75886—
ReactantUrea, N-ethyl-N'-[4-[5,6,7,8-tetrahydro-4-[(3S)-3-Methyl-4-Morpholinyl]pyrido[3,4-d]pyriMidin-2-yl]phenyl]-HCID 46913570—
SolventDimethylformamideHCID 6228—
Product(S)-2-(2-(4-(3-ethylureido)phenyl)-4-(3-methylmorpholino)-5,6-dihydropyrido[3,4-d]pyrimidin-7(8H)-yl)-N,N-dimethylacetamideHCID 59239517—

Reaction Steps

(S)-1-ethyl-3-(4-(4-(3-methylmorpholino)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-2-yl)phenyl)urea (0.086 mmol), N,N-diisopropylaethylamine (0.26 mmol), potassium iodide (0.06 mmol) were mixed in DMF (0.4 mL), then 2-chloro-N,N-dimethylacetamide was added. The mixture was stirred at room temperature for ˜3 h and the product was purified by reverse-phase HPLC to give the desired product. LC-MS: m/z=+482 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163763B2
Source datasetuspto-grants-2012_04
ORD IDord-c903939e62d546ef916d8ba234804d50
Source noteuspto-grants-2012_04