HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872323Generated: October 30, 2026
Potassium Carbonate → {1-[4-(3-Phenyl-6-vinyl-imidazo[1,2-a]pyridin-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/872323
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tri(butyl)vinylstannane | HCID 21115800 | — |
| Reactant | Tert-butyl {1-[4-(6-bromo-3-phenylimidazo[1,2-a]pyridin-2-yl)phenyl]cyclobutyl}carbamate | HCID 66665495 | — |
| Catalyst | Tetraethylammonium Bromide | HCID 6285 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {1-[4-(3-Phenyl-6-vinyl-imidazo[1,2-a]pyridin-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester | HCID 66665743 | — |
Reaction Steps
A mixture of {1-[4-(6-bromo-3-phenyl-imidazo[1,2-a]pyridin-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester (70 mg, 60% purity by UPLC-MS), potassium carbonate (11.2 mg), tetraethylammonium bromide (22.1 mg), tributylvinyl stannane (38.5 mg) and trans-dichlorobis(triphenylphosphine) palladium (II) (1.7 mg) in THF (0.66 mL) under argon was heated at 120° C. for 45 min. On cooling the reaction was partitioned between DCM and water, the organic extract dried and concentrated to give the crude title compound which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08975265B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-d2c280c6d2174654aa5897fb9bdb1fd9 |
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| Source note | uspto-grants-2015_03 |
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