HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386093Generated: October 31, 2026
2-Methyl-2-butanol → HCID 59525788, compound
https://huagongshe.com/reaction/386093
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methyl-2-butanol | HCID 6405 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | 2-Amino-5-[2,6-difluoro-4-(1-hydroxy-1-methylethyl)phenyl]thiophene-3-carboxamide | HCID 59525619 | — |
| Reactant | HCID 59526076 | HCID 59526076 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Product | HCID 59525788 | HCID 59525788 | — |
Reaction Steps
2-Amino-5-[2,6-difluoro-4-(1-hydroxy-1-methylethyl)phenyl]thiophene-3-carboxamide (85 mg, 0.272 mmol), (4-chloropyrimidin-2-yl)methyl methylcarbamate (54.9 mg, 0.272 mmol), Pd2 dba3 (24.92 mg, 0.027 mmol), K2CO3 (41.4 mg, 0.299 mmol) and X-Phos (64.9 mg, 0.136 mmol) were added to a 5 mL microwave vial. Degassed tert-amyl alcohol (0.6 mL) was added and the vial evacuated and back-filled with N2 (3×). The resulting mixture was stirred at 100° C. overnight. The reaction mixture was cooled to room temperature, MeOH and silica gel were added, and the solvent was removed in vacuo. Purification of the residue twice by silica gel chromatography (0-10% MeOH-DCM) gave [4-({3-(aminocarbonyl)-5-[2,6-difluoro-4-(1-hydroxy-1-methylethyl)phenyl]-2-thienyl}amino)pyrimidin-2-yl]methyl methylcarbamate as a beige solid after triturating in DCM.
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-972f4e2ae8144364b1fafb59766cc7c3 |
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| Source note | uspto-grants-2013_02 |
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