Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422532Generated: November 2, 2026

Hydrate;hydrochloride → 8-Chloro-2-(4-isopropyl-thiazol-2-yl)-7-(2-morpholin-4-yl-ethoxy)-quinolin-4-ol

https://huagongshe.com/reaction/1422532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrate;hydrochlorideHCID 21885828—
ReactantHCID 178496099HCID 178496099—
SolventAcetic AcidHCID 176—
Product8-Chloro-2-(4-isopropyl-thiazol-2-yl)-7-(2-morpholin-4-yl-ethoxy)-quinolin-4-olHCID 178439802—

Reaction Conditions

Temperature60 °C

Reaction Steps

8-Chloro-7-(2,2-dimethoxy-ethoxy)-2-(4-isopropyl-thiazol-2-yl)-quinolin-4-ol (5.0 g, 12.3 mmol) was dissolved in HOAc (100 mL) and 1.4 N HCl/H2O (50 mL). The reaction mixture was heated to 60° C. with stirring for 2 hrs. After cooled back to room temperature and concentrated, the residue was co-evaporated with toluene (2×50 mL). Then the crude was dissolved in DCM (100 mL) and cooled to 0° C. with stirring. Morphiline (1.6 g, 18.4 mmol) and NaHB(OAc)3 (3.9 g, 18.4 mmol) were added to the reaction mixture. After stirring at room temperature for 1 h, the reaction mixture was washed with sat. NaHCO3, brine and dried by Na2SO4. After concentration, the crude was purified by silica gel chromatography to afford 5.0 g of 8-chloro-2-(4-isopropyl-thiazol-2-yl)-7-(2-morpholin-4-yl-ethoxy)-quinolin-4-ol as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927484B2
Source datasetuspto-grants-2015_01
ORD IDord-81da5162534242298dab728203f48977
Source noteuspto-grants-2015_01