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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528140Generated: November 3, 2026

Sodium hydride → Tert-butyl 3-((5-aminopyrimidin-4-yl)oxy)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/1528140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-Boc-3-pyrrolidinolHCID 4416939—
Reactant4-Chloropyrimidin-5-amineHCID 13404541—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 3-((5-aminopyrimidin-4-yl)oxy)pyrrolidine-1-carboxylateHCID 86720863—

Reaction Conditions

Temperature100 °C

Reaction Steps

At room temperature, NaH (71 mg, 2.94 mmol) was added to a solution of tert-butyl-3-hydroxypyrrolidine-1-carboxylate (1B2) (500 mg, 2.67 mmol) in THF (tetrahydrofuran) (10 mL) and stirred for 1 hour. 4-chloropyrimidin-5-amine (H) (348 mg, 2.67 mmol) was then added. The reaction mixture was then heated to 100° C. under nitrogen and stirred for 4 hours, cooled to room temperature (20-30° C.) and concentrated in vacuo. The residue was purified with flash column (eluent: 10-30% ethyl acetate/petroleum ether) to obtain the product 1D3 (336 mg, 1.2 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090594B2
Source datasetuspto-grants-2015_07
ORD IDord-969267a84497407caaa7e4c83b1e3917
Source noteuspto-grants-2015_07