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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658358Generated: October 26, 2026

Benzylamine → 6-chloro-1-hydroxy-2-(trifluoromethyl)-1H-imidazo(4,5-b)pyridine benzylamine salt

https://huagongshe.com/reaction/1658358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
Reactant1-HydroxyfluromidineHCID 3082418—
SolventEthyl AcetateHCID 8857—
Product6-chloro-1-hydroxy-2-(trifluoromethyl)-1H-imidazo(4,5-b)pyridine benzylamine saltHCID 20355464—

Reaction Steps

6-CHLORO-1-hydroxy-2-(Trifluoromethyl)-1H-imidazo(4,5-b)-pyridine (1.4 grams) was mixed with 15 milliliters of ethyl acetate. The mixture was heated to reflux, and 0.6 milliliter of benzylamine was added dropwise. The mixture was then refluxed for another 30 minutes, cooled, and filtered, yielding the desired 6-chloro-1-hydroxy-2-(trifluoromethyl)-1H-imidazo(4,5-b)pyridine benzylamine salt, m.p., 200°-02°C. NMR analysis in hexadeuterodimethyl sulfoxide showed a peak at 236 cps (2H); a peak at 437 cps (5H); two meta-coupled doublets at the 462 cps (1H), the other at 500 cps (1H); and a broad peak at 474 cps (3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03963734
Source datasetuspto-grants-1976_06
ORD IDord-2e72d331ad1840efb9851f5e482aa78d
Source noteuspto-grants-1976_06