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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697948Generated: October 29, 2026

Methyl iodide → HCID 59239140, compound

https://huagongshe.com/reaction/1697948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 59239135HCID 59239135—
ReactantHCID 59239154HCID 59239154—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 59239140HCID 59239140100%

Reaction Steps

Step 1—Synthesis of (S)-6-(benzyloxy)-N-(4-(7-methyl-4-(3-methylmorpholino)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-2-yl)phenyl)pyridin-2-amine (mt): (S)-6-(benzyloxy)-N-(4-(4-(3-methylmorpholino)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-2-yl)phenyl)pyridin-2-amine (ms) (100 mg, 0.2 mmol) was dissolved in DMF (2 mL) and DIPEA (159 μL, 0.9 mmol)). To this solution was added MeI (14 μL, 0.2 mmol) at rt. The resulting solution was stirred at rt for 4 hrs. It was diluted with H2O, extracted with EtOAc (2×10 mL). The combined organics were washed with brine, dried over Magnesium sulfate, filtered, concentrated in vacuo to afford 100 mg (100%) of the title compound mt. LC-MS: m/z=+524 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163763B2
Source datasetuspto-grants-2012_04
ORD IDord-018def37e6a04a619b1a77d0958f053b
Source noteuspto-grants-2012_04