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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260192Generated: October 31, 2026

Methyl iodide → 1-Methyl-3-{N-[beta-(4-pivalyloxyphenyl)ethyl]}carbamoylpyridinium iodide

https://huagongshe.com/reaction/260192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant3-{N-[beta-(4-pivalyloxyphenyl)ethyl]}carbamoylpyridineHCID 13473427—
SolventAcetoneHCID 180—
Product1-Methyl-3-{N-[beta-(4-pivalyloxyphenyl)ethyl]}carbamoylpyridinium iodideHCID 13473429—

Reaction Steps

To a solution of 1.63 g (5 mmol) of the product of Example 26 in 10 ml of acetone, 1.41 g (10 mmol) methyl iodide were added and the mixture was refluxed overnight while stirring. The acetone layer was separated by decantation and the yellowish, oily residue was crystallized from methanol/ether. Yield, 1.94 g (83%), m.p. 155°-157° C. PMR (D2O) δ 9.16-8.00 (m, 4H, C5H4N+), 7.33-6.83 (m, 4H, C6H4), 4.40 (s, 3H, N+ --CH3), 3.5 (t, 2H, J=7 Hz, ##STR1455## 2.90 (t, 2H, J=7 Hz, CH2), 1.30 (s, 9H, C--(CH3)3). Anal. (C20H25N2O3I) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05525727
Source datasetuspto-grants-1996_06
ORD IDord-a2b3fdab0f454883a7481ed903560e96
Source noteuspto-grants-1996_06