HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397182Generated: October 28, 2026
2-Aminothiazole → Rac-2-cyclopentyloxy-2-(3,4-dichloro-phenyl)-n-thiazol-2-yl-acetamide
https://huagongshe.com/reaction/397182
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Rac-cyclopentyloxy-(3,4-dichloro-phenyl)-acetic acid | HCID 12044174 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Rac-2-cyclopentyloxy-2-(3,4-dichloro-phenyl)-n-thiazol-2-yl-acetamide | HCID 9947591 | 71.3% |
Reaction Steps
A solution of rac-cyclopentyloxy-(3,4-dichloro-phenyl)-acetic acid (52 mg, 0.17 mmol) in dichloromethane (10 mL) was treated with O—(1H-benzotriazolo-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (HBTU) (72 mg, 0.19 mmol), diisopropyl-ethylamine (0.09 mL, 0.52 mmol) and 2-aminothiazole (26 mg, 0.25 mmol). The resulting brownish-orange solution was then stirred 16 h at 25° C. The reaction was then diluted with water (10 mL) and extracted with ethyl acetate (3×15 mL). The combined organic layers were washed with water (1×10 mL), 1N sodium hydroxide solution (1×10 mL), 1N hydrochloric acid (1×10 mL) and brine (1×10 mL), then were dried over sodium sulfate and concentrated in vacuo. The product was purified by flash chromatography (Merck Silica gel 60, 230-400 mesh, 90/10 hexanes/ethyl acetate) to furnish rac-2-cyclopentyloxy-2-(3,4-dichloro-phenyl)-N-thiazol-2-yl-acetamide (45 mg, 70% yield) as a white foam: EI-HRMS m/e calcd for C16H16Cl2O2N2S (M+) 370.0309, found 370.0309.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06608218B2 |
|---|
| Source dataset | uspto-grants-2003_08 |
|---|
| ORD ID | ord-454df27118d14b0e874448347d72b337 |
|---|
| Source note | uspto-grants-2003_08 |
|---|