Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430542Generated: October 31, 2026

Ammonia → 2-Pentylthiazolo[4,5-c]quinolin-4-amine

https://huagongshe.com/reaction/430542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantDichloromethaneHCID 6344—
ReactantHCID 22648316HCID 22648316—
SolventMethanolHCID 887—
Product2-Pentylthiazolo[4,5-c]quinolin-4-amineHCID 9838345—

Reaction Steps

Trichloroacetyl isocyanate (0.51 mL) was added to a solution of 2-pentylthiazolo[4,5-c]quinoline-5N-oxide (0.78 g) in dichloromethane (50 mL). The reaction mixture was stirred at ambient temperature for about 75 minutes and then concentrated under vacuum to provide crude N-(2-pentylthiazolo[4,5-c]quinolin-4-yl)trichloroacetamide. The amide was combined with a solution of ammonia in methanol (40 ml of 2M). Dichloromethane was added to bring all of the material into solution. When the reaction was completed as indicated by thin layer chromatography, the reaction a mixture was concentrated under vacuum. The residue was mixed with dichloromethane and sodium bicarbonate. The organic layer was separated, washed with sodium bicarbonate then with water, dried over magnesium sulfate and then concentrated under vacuum to provide a white solid. This material was recrystallized from ethyl acetate to provide 2-pentylthiazolo[4,5-c]quinolin-4-amine as an off-white crystalline solid, m.p. 119-121° C. Analysis: Calculated for C15H17N3S: % C, 66.39; % H, 6.31; % N, 15.48; Found: % C, 66.21; % H, 6.35; % N, 15.39.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06323200B1
Source datasetuspto-grants-2001_11
ORD IDord-f3a1b98bc7cd457c9dca07fcdc3a0722
Source noteuspto-grants-2001_11