HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255055Generated: October 25, 2026
2-Bromoethyl methyl ether → 5-(4-fluoro-benzyl)-3-(2-methoxyethyl)-3H-thiazol-2-ylidene-amine
https://huagongshe.com/reaction/255055
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromoethyl methyl ether | HCID 80972 | — |
| Reactant | 5-(4-Fluoro-benzyl)-thiazol-2-ylamine | HCID 703479 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-(4-fluoro-benzyl)-3-(2-methoxyethyl)-3H-thiazol-2-ylidene-amine | HCID 66859070 | 80.8% |
Reaction Steps
A mixture of 5-(4-fluoro-benzyl)-thiazol-2-ylamine (330 mg, 1.59 mmol) and 2-bromoethyl methyl ether (0.50 mL, 5.34 mmol) was heated to 85° C. and stirred for 12 hours. The mixture was cooled to ambient temperature, diluted with 20 mL of ethyl acetate and washed with saturated aqueous NaHCO3. The layers were separated and the aqueous phase was extracted with 2×20 mL ethyl acetate and the combined organic extracts were dried over anhydrous Na2SO4, filtered, and concentrated. Purification by column chromatography (SiO2, 50% ethyl acetate in dichloromethane containing 0.5% Et3N) afforded 342 mg of the title compound: MS (LC/MS) m/z 267 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07875639B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-c680b71a2f4b43e597cd2c59e49a9964 |
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| Source note | uspto-grants-2011_01 |
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