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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099125Generated: November 2, 2026

Hydrochloric Acid → 2-(4-Isopropylthiazol-2-YL)-7-methoxy-8-methylquinolin-4-OL

https://huagongshe.com/reaction/1099125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantN-(6-Acetyl-3-methoxy-2-methylphenyl)-4-(propan-2-yl)-1,3-thiazole-2-carboxamideHCID 53482122—
SolventDiethyl EtherHCID 3283—
Solventtert-ButanolHCID 6386—
Product2-(4-Isopropylthiazol-2-YL)-7-methoxy-8-methylquinolin-4-OLHCID 17848769289.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

Potassium tert-butoxide (21.8 g, 195 mmol) was added to a suspension of the compound 5 (30.8 g, 92.7 mmol) in tert-butanol. The resulting reaction mixtures was heated at 100° C. overnight. Then, the reaction mixture was cooled at room temperature and diluted with ether (100 mL). The precipitate was filtered off and washed with Et2O to give a powder (fraction A). The mother liquor was concentrated in vacuo, triturated in ether, filtered off, and washed with ether to give a powder (fraction 2). Fractions 1 and 2 were mixed and poured into water (250 mL). The pH of the resulting solution was adjusted to 6-7 (control with pH paper) with HCl 1N. The precipitate was filtered off, washed with water and dried. Then, the solid was triturated in diisopropyl ether, filtered off and dried to give 26 g (88%) of the compound 6 as a brownish solid: m/z=315 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143402B2
Source datasetuspto-grants-2012_03
ORD IDord-0999a707b5e24a019cad801ef3ef865f
Source noteuspto-grants-2012_03