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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426370Generated: November 2, 2026

Methanamine, N-methoxy-, hydrochloride (1:1) → HCID 57608090, compound

https://huagongshe.com/reaction/2426370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
Reactant1-{[4-amino-2-(chloromethyl)-1H-imidazo[4,5-c]quinolin-1-yl]methyl}cyclobutanolHCID 57515522—
ReactantHCID 67262971HCID 67262971—
ProductHCID 57608090HCID 57608090—

Reaction Steps

1-[(4-Amino-2-{[methoxy(methyl)amino]methyl}-1H-imidazo[4,5-c]quinolin-1-yl)methyl]cyclobutanol was prepared according to the general methods of Part I of Example 9 using N,O-dimethyl hydroxylamine hydrochloride in lieu of methoxylamine hydrochloride and using 1-{[4-amino-2-(chloromethyl)-1H-imidazo[4,5-c]quinolin-1-yl]methyl}cyclobutanol in lieu of 2-(chloromethyl)-1-isobutyl-6,7-dimethyl-1H-imidazo[4,5-c]pyridin-4-amine hydrochloride. The crude product was purified by HPFC eluting with a gradient of 0-35% CMA in chloroform and then recrystallized from acetonitrile to provide pure product as a white powder, mp 219.0-221.0° C. Anal. Calcd for C18H23N5O2 C, 63.32; H, 6.79; N, 20.51. Found: C, 63.12; H, 6.56; N, 20.16.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968563B2
Source datasetuspto-grants-2011_06
ORD IDord-cd25fff9842f4aca960e041d39ea1190
Source noteuspto-grants-2011_06