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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098753Generated: November 1, 2026

Methyl iodide → HCID 86618416, compound

https://huagongshe.com/reaction/2098753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant(2-Chloro-4-morpholinothieno[3,2-d]pyrimidin-6-yl)methanolHCID 46180605—
SolventDimethylformamideHCID 6228—
ProductHCID 86618416HCID 86618416—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (2-chloro-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-6-yl)-methanol (300 mg) in DMF (10 mL) at 0° C. was added sodium hydride (46 mg). The mixture was stirred for 1 h at 0° C. and then methyliodide (0.07 mL) was added. The reaction mixture was stirred at room temperature for 16 h and then quenched with water (20 mL) and extracted into ethyl acetate (2×20 mL). The combined organics were washed with aqueous brine solution (2×20 mL), dried (MgSO4) and concentrated to give 2-chloro-6-methoxymethyl-4-morpholin-4-yl-thieno[3,2-d]pyrimidine as a yellow solid (92 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450315B2
Source datasetuspto-grants-2013_05
ORD IDord-2352f7217f4543b5bbb2a13eaa10ae2b
Source noteuspto-grants-2013_05