HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389994Generated: November 1, 2026
Boron tribromide → HCID 51356770, compound
https://huagongshe.com/reaction/389994
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 67116145 | HCID 67116145 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 51356770 | HCID 51356770 | — |
Reaction Steps
A commercial solution of boron tribromide (1N in DCM, 0.84 mL, 0.84 mmol) was added to a solution of 2-[4-(4-(4-ethyl-5-fluoro-2-methoxyphenoxy)-3-fluorobenzoyl]-2-oxopiperazin-1-yl)acetamide (which may be prepared in accordance with the experimental described in Example 6, step 1; 140 mg, 0.31 mmol) in dichloromethane (1 mL) placed under argon at −30° C. The reaction mixture was stirred at room temperature overnight and diluted by addition of dichloromethane (20 mL) and a saturated solution of ammonium chloride (20 mL). After separation, the aqueous layer was extracted with dichloromethane (2×20 mL). The combined organic phases were dried over sodium sulfate, filtered and concentrated under vacuum. The residue was purified by chromatography on silica gel, using dichloromethane/methanol (95:5 to 90:10) as eluent. The title product was obtained as a white solid (30 mg, 22%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383621B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-74b534a1675c4a2aae670a692ef6b166 |
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| Source note | uspto-grants-2013_02 |
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