HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481203Generated: November 1, 2026
Phosphorus oxybromide → HCID 89812986, compound
https://huagongshe.com/reaction/1481203
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxybromide | HCID 24613 | — |
| Reactant | HCID 178450861 | HCID 178450861 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 89812986 | HCID 89812986 | 74% |
Reaction Steps
To a mixture of 7-cyclohexylsulfanyl-1,4-dihydroxy-isoquinoline-3-carboxylic acid butyl ester (2.95 g, 7.87 mmol) in toluene (40 mL) was added POBr3 (3.38 g, 11.8 mmol) was refluxed for 3 h. Reaction mixture was cooled to 0° C. and quenched with saturated NaHCO3 aqueous solution (100 mL). It was stirred for 15 min., and then was extracted with EtOAc. Organic layer was washed with brine, dried over MgSO4, filtered and concentrated to provide the title compound 2.55 g (5.82 mmol), which was used directly to the next reaction without further purification. 1H NMR (200 MHz) CDCl3, δ in ppm: 11.85 (s, 1H), 8.23 (d, J=8.8 Hz, 1H), 8.05 (s, 1H), 7.65 (d, J=8.5 Hz, 1H), 4.47 (t, J=7.0 Hz, 2H), 3.46 (br S, 1H), 2.10 (br m, 2H), 1.85-1.42 (m, 12H), 0.99 (t, J=7.1 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409892B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-0670db69a61849de97a30cea31bef1bd |
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| Source note | uspto-grants-2016_08 |
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