HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402107Generated: October 31, 2026
Tetrahydrofuran → Ethyl 2-(2-acetamidopyridin-4-yl)-4-(naphthalen-2-ylmethyl)thiazole-5-carboxylate
https://huagongshe.com/reaction/2402107
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl 2-(2-acetamidopyridin-4-yl)-4-bromothiazole-5-carboxylate | HCID 66747706 | — |
| Reactant | HCID 178419770 | HCID 178419770 | — |
| Catalyst | HCID 178418851 | HCID 178418851 | — |
| Product | Ethyl 2-(2-acetamidopyridin-4-yl)-4-(naphthalen-2-ylmethyl)thiazole-5-carboxylate | HCID 66747854 | 40% |
Reaction Steps
To a mixture of ethyl 2-(2-acetamidopyridin-4-yl)-4-bromothiazole-5-carboxylate (190 mg, 0.510 mmol) and bis(tri-t-butylphosphine)palladium(0) (65.6 mg, 0.128 mmol) under nitrogen was added a 0.500 M solution of 2-napthylmethylzinc bromide in THF (3.60 mL, 1.80 mmol). The reaction was stirred at room temperature for 5 minutes, then at 60 degrees for 1 hour. Another portion of bis(tri-t-butylphosphine)palladium(0) (60.0 mg, 0.117 mmol) was added, followed by another portion of 0.500 M solution of 2-napthylmethylzinc bromide in THF (3.00 mL, 1.50 mmol), and the reaction was heated at 60 degrees for an additional 45 minutes. The reaction was cooled to room temperature and quenched with saturated ammonium chloride (10 mL). The mixture was extracted with ethyl acetate (2×20 mL) and the combined organic layers were dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography (ethyl acetate/hexane=0/100→100/0) to give 100 mg of the title compound. (40% yield). LC/MS (FA) ES+ 432.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08796271B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-96c856dddf0248b09eb0f42e1b736aec |
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| Source note | uspto-grants-2014_08 |
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