HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 913351Generated: November 2, 2026
Hydrogen Bromide → HCID 136367418, compound
https://huagongshe.com/reaction/913351
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 67392996 | HCID 67392996 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 136367418 | HCID 136367418 | 82% |
Reaction Steps
To 7-benzyloxy-2-propylthiazolo[4,5-c]quinoline (prepared as described in Part F of Example 1, 4.52 g, 13.5 mmol) was added a 45 wt. % solution of hydrogen bromide in acetic acid (40 mL). The resulting solution was heated at 65° C. for 1.5 h, then cooled in an ice bath. Aqueous NaOH (50% w/w solution) was added slowly until the pH=7 and a light yellow solid formed. The solid was isolated by filtration, dried, and then suspended in boiling ethanol (25 mL) for 5 min. The mixture was allowed to cool to rt and a tan solid was isolated by filtration. The solid was washed with cold ethanol and dried in a vacuum oven to yield 7-hydroxy-2-propylthiazolo[4,5-c]quinoline (2.69 g, 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08026366B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-86c787645f2248baaa098025af739f07 |
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| Source note | uspto-grants-2011_09 |
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