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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085174Generated: October 30, 2026

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

https://huagongshe.com/reaction/1085174

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, ##STR1473## 7.33-6.83 (m 4H, C6H4), 4.40 (s, 3H, N--CH3), 3.5 (t, 2H, J=7 Hz, ##STR1474## 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 numberUS05008257
Source datasetuspto-grants-1991_04
ORD IDord-595c9dd530824736a6cb764eed6ba442
Source noteuspto-grants-1991_04