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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885587Generated: November 1, 2026

Potassium Iodide → HCID 19879235, compound

https://huagongshe.com/reaction/1885587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant1-BromopropaneHCID 7840—
ReactantSodium hydrideHCID 24758—
ReactantHCID 136403394HCID 136403394—
SolventDimethylformamideHCID 6228—
ProductHCID 19879235HCID 19879235—

Reaction Steps

A stirred solution of 1.2 g (2.7 mmoles) of 2-(4-hydroxyphenyl) 3-(4-pyridyl)-6,7-dihydro[5H]-pyrrolo-[1,2-a]imidazole dihydrobromide of Example 10 in 20 ml of dry dimethylformamide cooled in an ice bath was treated with 360 mg (9.0 mmoles) of 60% sodium hydride dispersion and allowed to warm to room temperature. 450 mg (2.7 mmoles) of powdered potassium iodide was added, followed by dropwise addition of a solution of 332 mg (2.7 mmoles) of 1-propyl bromide in 2 ml of dimethylformamide. After 2 hours an additional 83 mg (0.67 mmole) of 1-propyl bromide was added followed by another 90 mg (2.25 mmoles) of 60% sodium hydride suspension, and the mixture heated to 65° C. for 2.5 hours. After stirring overnight, the mixture was poured into 10 volumes of ice water and extracted three times with ethyl acetate. The organic phase was washed with water, dried over anhydrous potassium carbonate and concentrated in vacuo. The residue was flash chromatographed on silica and the fractions eluting with 3 to 6% methanol in chloroform were combined, concentrated in vacuo, and recrystallized from ethyl acetate to afford the titled compound, mp 148.5°-150° C. Anal. Calcd. for C20H21N3O: C, 75.21; H, 6.63; N, 13.16. Found: C, 74.95; H, 6.59; N, 13.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05145858
Source datasetuspto-grants-1992_09
ORD IDord-760c34596796495689ce51ff20105554
Source noteuspto-grants-1992_09