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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502154Generated: October 29, 2026

Methyl iodide → Methyl 2-(2-(1H-tetrazol-1-yl)pyrimidin-5-yl)propanoate

https://huagongshe.com/reaction/1502154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 2-(2-(1H-tetrazol-1-yl)pyrimidin-5-yl)acetateHCID 89619075—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductMethyl 2-(2-(1H-tetrazol-1-yl)pyrimidin-5-yl)propanoateHCID 89618816—

Reaction Steps

To a suspension of sodium hydride (60% dispersion in mineral oil) (19.1 mg, 0.477 mmol) in anhydrous DMF (3.2 mL) was added solution of methyl 2-(2-(1H-tetrazol-1-yl)pyrimidin-5-yl)acetate (100 mg, 0.454 mmol) in anhydrous DMF (1.4 mL) at room temperature. Stirred for 10 min, then added methyl iodide (42.6 μl, 0.681 mmol) dropwise. Stirred at room temperature for 1 h. Reaction mixture was diluted with ethyl acetate and washed with water (3 times). Organic layer was washed with brine, dried over anhydrous magnesium sulfate and concentrated. The residue was purified by MPLC, eluting with 20-100% ethyl acetate/hexanes, 26 column volumes. LC/MS: [(M+1)]+=235.2;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206199B2
Source datasetuspto-grants-2015_12
ORD IDord-b93b350cc2bf4c908754fb07c8ad92d0
Source noteuspto-grants-2015_12