HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484471Generated: October 30, 2026
Pyridinium hydrobromide → HCID 71576560, compound
https://huagongshe.com/reaction/1484471
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridinium hydrobromide | HCID 21226041 | — |
| Reactant | HCID 89587862 | HCID 89587862 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 71576560 | HCID 71576560 | — |
Reaction Steps
To a stirred suspension of 4-(2-aminoethoxy)-7-fluoro-3-(4-pyrrolidin-1-yl-phenyl)-2H-isoquinolin-1-one hydrochloride [(I), cpd. 7, R=R1=R2=H, R3=4-pyrrolidin-1-yl, R4=H](15 mg, 0.037 mmol) in dry THF (0.3 mL), kept at room temperature, pyridinium hydrobromide perbromide (13 mg, 0.04 mmol) were added. The reaction mixture was stirred for 1 hour, the volatiles were then evaporated in vacuo and the resulting crude was purified through preparative HPLC on a Phenomenex Gemini C18 (21×250 mm, 10 μm) column, using a Waters FractionLynx System equipped with a 2996 PDA detector and ZQ2000 single quadrupole mass spectrometer, with electrospray ionization (positive and negative mode). Mobile phase A was 0.05% NH3/ACN 95/5, and mobile phase B was ACN. Gradient from 5 to 95% B in 25 min, hold 95% B 3 min. Flow rate 20 mL/min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422243B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-f9e90302756e42e284a13e83da0b908e |
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| Source note | uspto-grants-2016_08 |
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