HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430356Generated: October 29, 2026
Ammonium Hydroxide → 3-cyclopentyl-2-(3-hydroxy-phenyl)-N-thiazol-2-yl-propionamide
https://huagongshe.com/reaction/430356
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 3-cyclopentyl-2-(3-methoxy-phenyl)-N-thiazol-2-yl-propionamide | HCID 22315281 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-cyclopentyl-2-(3-hydroxy-phenyl)-N-thiazol-2-yl-propionamide | HCID 22315113 | 45.1% |
Reaction Steps
A 1.0M solution of boron tribromide in methylene chloride (3.53 mL, 3.53 mmol) at 25° C. was treated with a solution of 3-cyclopentyl-2-(3-methoxy-phenyl)-N-thiazol-2-yl-propionamide (prepared in Example 110, 0.11 g, 0.35 mmol) in methylene chloride (3.5 mL). This solution was stirred at 25° C. for 1 h. At this time, the reaction was cooled to −0° C. and treated with a dilute aqueous ammonium hydroxide solution. This mixture was stirred at 0° C. for 15 min. At this time, the aqueous layer was separated from the organic layer. The aqueous layer was extracted with chloroform (3×50 mL). The organics were dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 50/50 hexanes/ethyl acetate) afforded 3-cyclopentyl-2-(3-hydroxy-phenyl)-N-thiazol-2-yl-propionamide (50 mg, 44.7%) as a white solid: mp 177-179° C.; EI-HRMS m/e calcd for C17H20N2O2S (M+) 316.1245 found 316.1244.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06320050B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-8a9413a06e354e96aeb25e37b3c30fe2 |
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| Source note | uspto-grants-2001_11 |
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