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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383148Generated: October 30, 2026

Pyridinium chloride → HCID 86626164, compound

https://huagongshe.com/reaction/2383148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridinium chlorideHCID 10176127—
ReactantHCID 86626163HCID 86626163—
SolventTolueneHCID 1140—
ProductHCID 86626164HCID 86626164—

Reaction Steps

For Examples 70-72, the following procedure was used. Under a nitrogen atmosphere, the reagent from the table below (1.5 equivalents) and pyridine hydrochloride (0.01-0.02 equivalents) were added to a solution of tert-butyl{4-[3-amino-6-(benzyloxy)quinolin-4-ylamino]butyl}carbamate (29-36 mmol, 1 equivalent) in toluene (200 mL), and the reaction was heated at reflux for three to five hours. The toluene was removed under reduced pressure. The residue was dissolved in a small amount of toluene, which was removed under reduced pressure. This was repeated three times. The resulting solid was dried under high vacuum at 100° C. to provide the tert-butyl{4-(8-benzyloxy-1H-imidazo[4,5-c]quinolin-1-yl]butyl}carbamate with the substituent indicated in the table below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263594B2
Source datasetuspto-grants-2012_09
ORD IDord-674da7da1da84fb08aea5c958bbc267a
Source noteuspto-grants-2012_09