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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337579Generated: October 30, 2026

Methyl iodide → 1,1-Dimethylethyl N-cyclopropyl-N-[[6-(3-methoxypropyl)-8-quinolinyl]methyl]carbamate

https://huagongshe.com/reaction/337579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 66895821HCID 66895821—
SolventTetrahydrofuranHCID 8028—
Product1,1-Dimethylethyl N-cyclopropyl-N-[[6-(3-methoxypropyl)-8-quinolinyl]methyl]carbamateHCID 66896562—

Reaction Steps

To a solution of 1,1-dimethylethyl cyclopropyl{[6-(3-hydroxypropyl)-8-quinolinyl]methyl}carbamate (1 eq.) from the previous step in THF (0.3 M) was added sodium hydride (60% (w/w) dispersion in paraffin oil, 1.2 eq.). The resulting suspension was stirred at RT for 15 min before iodomethane (1.4 eq.) was added. The now yellow solution was stirred at RT for 12 h before the reaction was quenched with the addition of 1 N aq. NaOH. The aqueous layer was separated and back-extracted with ether. The combined organic extracts were washed further with water and brine, dried over Na2SO4, filtered and the filtrate concentrated in vacuo. Purification of the crude product thus obtained by way of flash chromatography (SiO2, 9:1 (v/v) Hex:EtOAc→EtOAc) afforded the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889714B2
Source datasetuspto-grants-2014_11
ORD IDord-b1697f09717644bab60ad8fe82cca778
Source noteuspto-grants-2014_11