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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559395Generated: October 31, 2026

Methyl iodide → HCID 59670972, compound

https://huagongshe.com/reaction/559395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 59671070HCID 59671070—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59670972HCID 5967097255.2%

Reaction Steps

To a solution of (S)-tert-butyl 4-((5R,7R)-7-hydroxy-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl)-3-methylpiperazine-1-carboxylate (0.098 g, 0.28 mmol) in THF (10 mL) were added NaH (60%, 50 mg, 1.25 mmol) and MeI (0.08 mL, 1.28 mmol). The mixture was stirred at room temperature overnight. The solution was removed and the residue was purified by silica gel chromatography, eluting with ethyl acetate to give (S)-tert-butyl 4-((5R,7R)-7-methoxy-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl)-3-methylpiperazine-1-carboxylate (0.056 g, 55%). 1H NMR (CDCl3, 400 MHz) δ 8.56 (s, 1H), 4.66 (m, 2H), 4.30-3.80 (m, 3H), 3.55 (s, 3H), 3.54-2.90 (m, 4H), 2.25 (m, 1H), 1.98 (m, 1H), 1.49 (s, 9H), 1.24 (d, J=12.4 Hz, 3H), 1.13 (d, J=7.2 Hz, 3H). MS (APCI+) [M+H]+363.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063050B2
Source datasetuspto-grants-2011_11
ORD IDord-75bb90dda5c24cd7ac237d47561e55c8
Source noteuspto-grants-2011_11