Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464367Generated: October 26, 2026

2-(3-Aminopropylamino)-3-methylpyridine → 2-[N-(3-aminopropyl)-N-methylamino]-4-methylpyridine

https://huagongshe.com/reaction/464367

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-Aminopropylamino)-3-methylpyridineHCID 14397354—
ReactantN-[3-(N-phenyl-N-pyrid-2-ylamino)propyl]phthalimideHCID 20186606—
Product2-[N-(3-aminopropyl)-N-methylamino]-4-methylpyridineHCID 20262898—

Reaction Steps

Substituting 2-bromo-4-methylpyridine (25.8 g) for 2-bromo-3-methylpyridine and using the corresponding molar proportions of the other reagents in the method of Example 36(i) gave 2-(3-aminopropylamino)-4-methylpyridine (16.1 g), bp 120°-24° C.; 0.01-0.02 mm Hg. (ii) Substituting 2-(3-aminopropylamino)-4-methylpyridine (7.5 g) for 2-(3-aminopropylamino)-3-methylpyridine and using corresponding molar proportions of the other reagents in the method of Example 36(ii) gave 2-[N-(3-aminopropyl)-N-methylamino]-4-methylpyridine (3.53 g) as an oil. (iii) Substituting 2-[N-(3-aminopropyl)-N-methylamino]-4-methylpyridine (1.0 g) for 2-[N-(3-aminopropyl)-N-methyl amino]-3-methylpyridine and using corresponding molar proportions of the other reagents in method of Example 36(iii) gave 2-[3-[N-methyl-N-(4-methylpyrid-2-yl)amino] propylamino]-5-(6-methylpyrid-3-ylmethyl)pyrimid-4-one 1H2O, 0.56 g (26%) mp indeterminate (from ethanol/water).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04547506
Source datasetuspto-grants-1985_10
ORD IDord-b1692146e1744c13999306301c92138c
Source noteuspto-grants-1985_10