HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523756Generated: October 30, 2026
Phosphorus oxybromide → HCID 86014622, compound
https://huagongshe.com/reaction/523756
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxybromide | HCID 24613 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178450845 | HCID 178450845 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86014622 | HCID 86014622 | 98.4% |
Reaction Steps
411 mg of 1,4-Dihydroxy-5-phenyl-isoquinoline-3-carboxylic acid butyl ester, from Example D-39c isomer B, was suspended in 15 ml of anhydrous acetonitrile. 2.0 g of phosphorous oxybromide was added and the reaction mixture was heated to reflux for 3.5 h. The reaction mixture was cooled and poured into 75 ml of 0° C. saturated aqueous sodium bicarbonate solution. The mixture was stirred for 5 min and then extracted with 75 ml portions of ethyl acetate three times. The combined organic fractions were washed with brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue (434 mg) was purified by chromatography on silica gel using a gradient of 0 to 25% ethyl acetate in hexanes to elute the product as one major fraction. 480 mg of the desired product was obtained; MS (+): m/z 422.02 (M+23)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09339527B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-38481ed088a042d099947279ebcef7f4 |
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| Source note | uspto-grants-2016_05 |
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