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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393930Generated: October 30, 2026

Hydrochloric Acid → 2-Benzylthiazolo[4,5-c]quinolin-4-amine hydrochloride

https://huagongshe.com/reaction/393930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 22648314HCID 22648314—
SolventMethanolHCID 887—
SolventIsopropanolHCID 3776—
Product2-Benzylthiazolo[4,5-c]quinolin-4-amine hydrochlorideHCID 22648269—

Reaction Steps

Trichloroacetyl isocyanate (1.2 mL, 10.3 mmol) was added to a solution of 2-benzylthiazolo[4,5-c]quinoline-5N-oxide (2.0 g, 6.8 mmol) in dichloromethane (100 mL). The reaction mixture was stirred at ambient temperature for 2 hours and then concentrated to provide crude N-(2-benzylthiazolo[4,5-c]quinolin-4-yl)trichloroacetamide. The amide was dissolved in methanol. Sodium methoxide (1 equivalent) was added. The reaction mixture was heated on a steam bath for 30 minutes and then allowed to cool to ambient temperature. The resulting precipitate was isolated by filtration and then suspended in a mixture of methanol and isopropanol. Hydrochloric acid (1 equivalent) was added and all of the solid dissolved initially. A white solid crystallized out. This material was isolated by filtration, washed with isopropanol and then dried to provide 1.5 g of 2-benzylthiazolo[4,5-c]quinolin-4-amine hydrochloride, m.p. 152-155° C. Analysis: Calculated for: C17H13N3S. HCl: % C, 62.28; % H, 4.30; % N, 12.82; Found: % C, 62.05; % H, 4.23; % N, 12.82.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809203B2
Source datasetuspto-grants-2004_10
ORD IDord-e3394796838c494a9d757ecaede52fc6
Source noteuspto-grants-2004_10