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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925770Generated: November 2, 2026

N-Methylbenzylamine → Benzenemethanamine, N-pentyl-

https://huagongshe.com/reaction/1925770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylbenzylamineHCID 7669—
Reactant1-BromopentaneHCID 8057—
ReactantSodium CarbonateHCID 10340—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium BicarbonateHCID 516892—
ReactantPotassium BicarbonateHCID 516893—
ReactantHCID 43774819HCID 43774819—
ProductBenzenemethanamine, N-pentyl-HCID 264905—

Reaction Steps

The present invention also provides a process for the synthesis of 3-[N-(methylpentyl)amino]propionic acid (III) wherein N-methylbenzylamine is reacted with 1-bromo pentane in presence of a base like potassium carbonate, sodium carbonate, sodium bicarbonate, potassium bicarbonate preferably potassium carbonate to get N-methyl, N-pentyl benzyl amine (VI) which is subjected to debenzylation using 10% Pd/C as catalyst in an alcoholic solvent to get N-methyl, N-pentylamine (V) which is isolated in pure form as an acid addition salt of an organic acid such as fumaric acid, citric acid, maleic acid, edetic acid preferably it is isolated as an oxalate salt. Compound (V) is reacted with methyl-3-halopropionate like methyl 3-chloro propionate, methyl-3-bromo propionate, methyl 3-iodo propionate more preferably methyl-3-bromo propionate in a suitable solvent preferably toluene in the presence of a base preferably potassium carbonate at a temperature ranging from 25° C. to 80° C. preferably at 70° C. to get 3-[N-(methylpentyl)amino]propionate (IV), which is further hydrolyzed to give 3-[N-(methylpentyl)amino]propionic acid hydrochloride (III) which is the key intermediate for the synthesis of Ibandronate sodium.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178712B2
Source datasetuspto-grants-2012_05
ORD IDord-b526f897437b421f9b39d539f1c5b8ad
Source noteuspto-grants-2012_05