HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386140Generated: October 30, 2026
Potassium Carbonate → 5-{[tert-Butyl(dimethyl)silyl]ethynyl}-2-{[6-(morpholin-4-ylmethyl)pyridin-2-yl]amino}thiophene-3-carboxamide
https://huagongshe.com/reaction/386140
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | 4-((6-Bromopyridin-2-yl)methyl)morpholine | HCID 23438147 | — |
| Reactant | 2-Amino-5-{[tert-butyl(dimethyl)silyl]ethynyl}thiophene-3-carboxamide | HCID 59526335 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Product | 5-{[tert-Butyl(dimethyl)silyl]ethynyl}-2-{[6-(morpholin-4-ylmethyl)pyridin-2-yl]amino}thiophene-3-carboxamide | HCID 59526210 | — |
Reaction Steps
4-[(6-Bromopyridin-2-yl)methyl]morpholine (Example 45, Step 1) (340 mg, 1.32 mmol), 2-amino-5-{[tert-butyl(dimethyl)silyl]ethynyl}thiophene-3-carboxamide (445 mg, 1.59 mmol), Pd2dba3 (121 mg, 0.13 mmol), X-Phos (315 mg, 0.66 mmol), and K2CO3 (201 mg, 1.46 mmol) were combined in a vial, sealed, and evacuated/backfilled with nitrogen. Degassed t-amyl alcohol (3.3 ml), and the reaction was vigorously stirred at 100° C. overnight. The reaction mixture was then diluted with MeOH, combined with silica, and evaporated. Flash chromatography (dry load, 0-10% MeOH/EtOAc) afforded the title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367706B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-c13545f2cc474191a87ad7a0a154d458 |
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| Source note | uspto-grants-2013_02 |
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