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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | N-(6-Acetyl-3-methoxy-2-methylphenyl)-4-(propan-2-yl)-1,3-thiazole-2-carboxamide | HCID 53482122 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 2-(4-Isopropylthiazol-2-YL)-7-methoxy-8-methylquinolin-4-OL | HCID 178487692 | 89.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143402B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-0999a707b5e24a019cad801ef3ef865f |
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| Source note | uspto-grants-2012_03 |
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