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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289539Generated: October 29, 2026

Water → 1-(4-Pyrimidinyl)-4-methyl-4-(ethoxycarbonyl)piperidine

https://huagongshe.com/reaction/2289539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantLithium diisopropylamideHCID 2724682—
Reactant1-(4-Pyrimidinyl)-4-(ethoxycarbonyl)piperidineHCID 22721957—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Pyrimidinyl)-4-methyl-4-(ethoxycarbonyl)piperidineHCID 18698036—

Reaction Steps

1-(4-pyrimidinyl)-4-(ethoxycarbonyl)piperidine (400 mg) in 4 ml tetrahydrofuran was cooled to -70° C and treated with a solution of lithium diisopropylamide (1.0 ml in THF), under an argon atmosphere. After stirring 1.5 hours 1.2 ml of a solution of 1 ml iodomethane in 10 ml THF was added and reaction mixture left to reach room temperature overnight. Water added and extracted twice with ethyl acetate. Organic extract washed with brine and dried over magnesium sulphate, filtered and evaporated to give 1-(4-pyrimidinyl)-4-methyl-4-(ethoxycarbonyl)piperidine (370 mg) as an oil; NMR (CDCl3): 1.24 (s, 3H), 1.28 (t, 3H), 1.38-1.51 (m,2H), 2.14-2.26 (m, 2H), 3.12-3.26 (m, 2H), 4.03-4.14 (m, 2H), 4.2(q,2H), 6.5 (dd, 1H), 8.17 (d. 1H), 8.57 (s, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093718
Source datasetuspto-grants-2000_07
ORD IDord-7cee8ec630e2401198303bb37e025e2a
Source noteuspto-grants-2000_07