HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026362Generated: November 1, 2026
Triethylamine → tert-butyl [(1S)-2-(4-{[5-(cyclopropylmethoxy)pyridin-2-yl]ethynyl}-3,5-difluorophenoxy)-1-methylethyl]carbamate
https://huagongshe.com/reaction/1026362
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Bromo-5-(cyclopropylmethoxy)pyridine | HCID 57821796 | — |
| Reactant | tert-butyl [(1S)-2-(4-ethynyl-3,5-difluorophenoxy)-1-methylethyl]carbamate | HCID 86666330 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | Triphenylphosphine palladium dichloride | HCID 13169693 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | tert-butyl [(1S)-2-(4-{[5-(cyclopropylmethoxy)pyridin-2-yl]ethynyl}-3,5-difluorophenoxy)-1-methylethyl]carbamate | HCID 86666329 | 35.9% |
Reaction Steps
A mixture of tert-butyl [(1S)-2-(4-ethynyl-3,5-difluorophenoxy)-1-methylethyl]carbamate (2.5 g), 2-bromo-5-(cyclopropylmethoxy)pyridine (1.8 g), copper iodide (I) (0.15 g), dichloropalladium-triphenylphosphine (1:2) (0.56 g) and triethylamine (2.2 mL) in toluene (20 mL) was stirred at 100° C. overnight under argon atmosphere. After cooling to room temperature, the mixture was filtered through a pad of Celite. The filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to afford the title compound (1.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08729102B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-3418d85dd2534fa4b0cb79079f66eb44 |
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| Source note | uspto-grants-2014_05 |
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