HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398631Generated: October 29, 2026
Boron tribromide → HCID 22315268, compound
https://huagongshe.com/reaction/398631
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 22315140 | HCID 22315140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22315268 | HCID 22315268 | 63.5% |
Reaction Steps
A solution 3-cyclopentyl-2-(4-methoxy-phenyl)-N-thiazol-2-yl-propionamide (prepared as in Example 115, 1.03 g, 3.12 mmol) in methylene chloride (31.26 mL) at 25° C. was treated with a 1.0M solution of boron tribromide in methylene chloride (31.26 mL, 31.26 mmol). This solution was stirred at 25° C. for 4 h. At this time, the reaction was cooled to 0° C. and was then quenched by the dropwise addition of a dilute aqueous ammonium hydroxide solution. The resulting solution was stirred at 0° C. for 15 min. This mixture was then poured into water (50 mL) and extracted with ethyl acetate (3×30 mL). The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 70/30 hexanes/ethyl acetate) afforded 3-cyclopentyl-2-(4-hydroxy-phenyl)-N-thiazol-2-yl-propionamide (626.8 mg, 63.4%) as a off-white solid: mp 198-200° C.; EI-HRMS m/e calcd for C17H20N2O2S (M+) 316.1245 found 316.1256.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610846B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-ced53855b0a845a5b39956f686cc70f9 |
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| Source note | uspto-grants-2003_08 |
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